ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_34400 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | CAACACTTTGGGAAGATGAGGTGGGCAGATCACTTGAAGTCAGGAGTTCGAGATCAGCCTGGCCAACATAGTGAAACGCCATCTCTACTAAAAATACAAAAATTAGTGGAGGCAGGCGCCTGTAATCCCAGCTACTCCAGAGGCTGAGGAACCAGAATGGCTGGAACACAGGAGGTGGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCAAAAAAAATAAAAATAAAAACATTGAAAATTTAAATATGGTTACAAAAAAACAGAAATGCTCAACCCTGTCAATGT... | CAACACTTTGGGAAGATGAGGTGGGCAGATCACTTGAAGTCAGGAGTTCGAGATCAGCCTGGCCAACATAGTGAAACGCCATCTCTACTAAAAATACAAAAATTAGTGGAGGCAGGCGCCTGTAATCCCAGCTACTCCAGAGGCTGAGGAACCAGAATGGCTGGAACACAGGAGGTGGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCAAAAAAAATAAAAATAAAAACATTGAAAATTTAAATATGGTTACAAAAAAACAGAAATGCTCAACCCTGTCAATGT... |
Task1_train_34401 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | TTTTTTTTAGGCGGCGCCTCGCTCTGTCGCCCAGGCTGGAGCACAGTGGTGTGATCTCAGCTCATCGCGACCTCCGCCTCCCAGGTTCAAGCAATTCTCTGCCTCAGCCTCCCAAGTAGCTGGGATACAGGCACCCGCCACCATGCCTGGCTAATTTTTCTTTTTTAGTAGAGACAGGGTTTCACCATCTTAGCCAGGCTGGTCGTGAATTCCTGACCCCATGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCAGCCTCAATGCTTTAATTTTTTAACATCTGAGTTGTTAAG... | TTTTTTTTAGGCGGCGCCTCGCTCTGTCGCCCAGGCTGGAGCACAGTGGTGTGATCTCAGCTCATCGCGACCTCCGCCTCCCAGGTTCAAGCAATTCTCTGCCTCAGCCTCCCAAGTAGCTGGGATACAGGCACCCGCCACCATGCCTGGCTAATTTTTCTTTTTTAGTAGAGACAGGGTTTCACCATCTTAGCCAGGCTGGTCGTGAATTCCTGACCCCATGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCAGCCTCAATGCTTTAATTTTTTAACATCTGAGTTGTTAAG... |
Task1_train_34402 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCCAAATTAGTTCAATATTTGAATTTTTTCTAATCTATTAATATATACAACAAAGATTGGATGCTATGGGATGGAACAACTCGCTCCTAAAGCTGGCAATGTACATCCTTATGCAGACATACAAACTATGTGTTGTATATTTTATTATACAGTAAGAATAGCTTATGGGTTGCATAACATCCTTAAATTATTTTCTGTATTTTATCCTTAGAATAACCCTGTGTGATAGATAATGGGAAAGGTATGGCTACATTTATTTTACCAATGAAGAAAATGAAGTGTAGAGTAGTCACCAAGCTTGAACTAGATCCTTGACCTTC... | GCCAAATTAGTTCAATATTTGAATTTTTTCTAATCTATTAATATATACAACAAAGATTGGATGCTATGGGATGGAACAACTCGCTCCTAAAGCTGGCAATGTACATCCTTATGCAGACATACAAACTATGTGTTGTATATTTTATTATACAGTAAGAATAGCTTATGGGTTGCATAACATCCTTAAATTATTTTCTGTATTTTATCCTTAGAATAACCCTGTGTGATAGATAATGGGAAAGGTATGGCTACATTTATTTTACCAATGAAGAAAATGAAGTGTAGAGTAGTCACCAAGCTTGAACTAGATCCTTGACCTTC... |
Task1_train_34403 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAATTTTTTTGTACTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCCGGCCACGTGTACTAAATTTTAATGCGAAAAGTTATACTTTACATAAATGCATTTCATAATGTATAAAGCTACCTAGTAATGTACCAAATATTTATAAACTGAATTTCTTCTCTGAGGTGGGAAATACGCATTTAGGTCATGATTTTATAACAATTTAGTAGAACTGTAATTTTCGTTTCTTTTTATGT... | TAATTTTTTTGTACTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCCGGCCACGTGTACTAAATTTTAATGCGAAAAGTTATACTTTACATAAATGCATTTCATAATGTATAAAGCTACCTAGTAATGTACCAAATATTTATAAACTGAATTTCTTCTCTGAGGTGGGAAATACGCATTTAGGTCATGATTTTATAACAATTTAGTAGAACTGTAATTTTCGTTTCTTTTTATGT... |
Task1_train_34404 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CATCAAGGAAAACATCAACTGAATGTGCATCTAGTACAGAAAATTCTTTCGTTGTCAGCAGTAGTTCAGTTTCTAATACCACTGTTGCTGGAACTCCCCCATACCCTACAAGTCGGAGGCAAACCTTTATTACTTTGGAGAAGTTTGATGGTTCAGAAAATAGACCTTTTAGTCCATCCCCCTTGAATAATATTTCATCAACTGTTACAGTGAAAAATAACCAGGAAACCATGATTAAAACAGATTTTCTACCAAAAGCAAAGCAAAGAGAAGGGACTTTTTCAAAATCTGATTCTGAAAAAATAGTGAATGGAACTAAG... | CATCAAGGAAAACATCAACTGAATGTGCATCTAGTACAGAAAATTCTTTCGTTGTCAGCAGTAGTTCAGTTTCTAATACCACTGTTGCTGGAACTCCCCCATACCCTACAAGTCGGAGGCAAACCTTTATTACTTTGGAGAAGTTTGATGGTTCAGAAAATAGACCTTTTAGTCCATCCCCCTTGAATAATATTTCATCAACTGTTACAGTGAAAAATAACCAGGAAACCATGATTAAAACAGATTTTCTACCAAAAGCAAAGCAAAGAGAAGGGACTTTTTCAAAATCTGATTCTGAAAAAATAGTGAATGGAACTAAG... |
Task1_train_34405 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCTTTGGTATCAGGATGATGGTGGCCTCATAAAAAGAGTTAGTGAGGATTCCCTCTTTTTCTATTGATTGGAATAGTTTCAGAAGGAATGGTACCAGCTCCTCTTTGTACCTCTGGTAGAATTCGGCTGTGAATTCATCTGGTCCTGGACTTTTTTTGGTTGAATAATATGCATTATATGTATATACCACATTTTGTTTATCCAGTTGACAGACATTTGGGTTGTTTCCACCATTTGCTATTACGAATAATGCTGCTGTGTCTGCAAGTTTTTATATGGATAGATGATTTCATTTCTCTTGTATATATACCTAGAAGTGG... | GCTTTGGTATCAGGATGATGGTGGCCTCATAAAAAGAGTTAGTGAGGATTCCCTCTTTTTCTATTGATTGGAATAGTTTCAGAAGGAATGGTACCAGCTCCTCTTTGTACCTCTGGTAGAATTCGGCTGTGAATTCATCTGGTCCTGGACTTTTTTTGGTTGAATAATATGCATTATATGTATATACCACATTTTGTTTATCCAGTTGACAGACATTTGGGTTGTTTCCACCATTTGCTATTACGAATAATGCTGCTGTGTCTGCAAGTTTTTATATGGATAGATGATTTCATTTCTCTTGTATATATACCTAGAAGTGG... |
Task1_train_34406 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CAGGCAGAGGGCTTGAGCCTAGGGGTTTGAGACCAGCCTGGGCAACATAGTGAGCCTCTACCAAAAAAAAAAAAAAAAAAATTAGCCTAGAATGGCATATACACCTGTAGTCCTAGCTATTCTGGTGGCTGAGGCTGGAGGATTGCTTGAGTCCATGAAGTCGAGACTGCAGCGAGCTGTGATCATGCCACCACACTGCAGCCTGGGTGATAGAGTGAGACCCTGTCTCTAAAAATAAAAAAAAAGTATTCTGTATTATTCTTTGTACTTCTACAATTTTGTATTTTACATCTAAATCTTTGGTACAGCTACAGTTTATG... | CAGGCAGAGGGCTTGAGCCTAGGGGTTTGAGACCAGCCTGGGCAACATAGTGAGCCTCTACCAAAAAAAAAAAAAAAAAAATTAGCCTAGAATGGCATATACACCTGTAGTCCTAGCTATTCTGGTGGCTGAGGCTGGAGGATTGCTTGAGTCCATGAAGTCGAGACTGCAGCGAGCTGTGATCATGCCACCACACTGCAGCCTGGGTGATAGAGTGAGACCCTGTCTCTAAAAATAAAAAAAAAGTATTCTGTATTATTCTTTGTACTTCTACAATTTTGTATTTTACATCTAAATCTTTGGTACAGCTACAGTTTATG... |
Task1_train_34407 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCAAAAAGAAAAAGAGTTAACAGTTACCAAAAAAGGAAATGGTACAGATAACTTTTGATTATCTTTAGGGCCCCAAACCATTTGGGCAATTAGGTTAGATGGAAAGTAGTATGTTTCCTAAGGAAGTTAAGTGTAGTTACAGCAAGACACAACCAGGATAGGCACCTGCCCTGAAACCCTTGAGGACTGCAAGAGAGACCTGTGGTGTTCCTCAAAAGGATGAGAAACCACCATCATTTTACCGCTAGTCTCTCAATGTCAAGCCCCTGAGAGATGATCCAAACAGGAGTTACAGGCATGAGCTTCAATCACACTGAGAA... | CCAAAAAGAAAAAGAGTTAACAGTTACCAAAAAAGGAAATGGTACAGATAACTTTTGATTATCTTTAGGGCCCCAAACCATTTGGGCAATTAGGTTAGATGGAAAGTAGTATGTTTCCTAAGGAAGTTAAGTGTAGTTACAGCAAGACACAACCAGGATAGGCACCTGCCCTGAAACCCTTGAGGACTGCAAGAGAGACCTGTGGTGTTCCTCAAAAGGATGAGAAACCACCATCATTTTACCGCTAGTCTCTCAATGTCAAGCCCCTGAGAGATGATCCAAACAGGAGTTACAGGCATGAGCTTCAATCACACTGAGAA... |
Task1_train_34408 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTAACCTGAACCAAAGGGCAAGTTATAAACAGGCAGACACGGCAGCACACTTATGGGGCACAAATCCCGTGTTAAAGTGGACATTTACTTACCGCACTCCTCATCTTTTGGAAATCCAGACAGTGAACCACACCAGGGAATTCACCGATCACTTTTCCAGCCAGGTAGTGACCTTTCTGCTTCTCATATGTCTCTTTGTATTTAAGCTGTAAAGTGGGTTAAACATTGAGAATCGCTGGAGTTTCCTAACCAGCCCCTTGATCCCCAGTAAAGACTCTCAAACTTAGGAGAGGAAAAGGTCATACTGACCTCACTGTTCA... | CTAACCTGAACCAAAGGGCAAGTTATAAACAGGCAGACACGGCAGCACACTTATGGGGCACAAATCCCGTGTTAAAGTGGACATTTACTTACCGCACTCCTCATCTTTTGGAAATCCAGACAGTGAACCACACCAGGGAATTCACCGATCACTTTTCCAGCCAGGTAGTGACCTTTCTGCTTCTCATATGTCTCTTTGTATTTAAGCTGTAAAGTGGGTTAAACATTGAGAATCGCTGGAGTTTCCTAACCAGCCCCTTGATCCCCAGTAAAGACTCTCAAACTTAGGAGAGGAAAAGGTCATACTGACCTCACTGTTCA... |
Task1_train_34409 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCGCTACAAAAAAAAAAAAAAAAGAGAGAGAGAGAGAGAAAAATTATTTTGGTGTTCACAGATATTATTGTTTTGATTATGTGCCAGTCATCTCTCTTGTATACAAGGTAGAAATAAAATTATTAAAGCTGCATAAATTCCTTACCTTTGTTTCTTATTAAAATTCTTTCAATAATCTGTTAAAGGACTTATCGGTTATGAAAAGTATAATTGGATTGAAGTATTTAAAATAATTTATAGGAAAGAGTTATAGCACACAGTATTTTTTTTTTTTTGACAACCTACTAATCCAATCAGAAGCACACAGTACTTTAGGCTGG... | GCGCTACAAAAAAAAAAAAAAAAGAGAGAGAGAGAGAGAAAAATTATTTTGGTGTTCACAGATATTATTGTTTTGATTATGTGCCAGTCATCTCTCTTGTATACAAGGTAGAAATAAAATTATTAAAGCTGCATAAATTCCTTACCTTTGTTTCTTATTAAAATTCTTTCAATAATCTGTTAAAGGACTTATCGGTTATGAAAAGTATAATTGGATTGAAGTATTTAAAATAATTTATAGGAAAGAGTTATAGCACACAGTATTTTTTTTTTTTTGACAACCTACTAATCCAATCAGAAGCACACAGTACTTTAGGCTGG... |
Task1_train_34410 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AACAATATTTTCCTTGCTGGTGGCACAAAGCCAGGTGAAATAACTAACACATCAGCTGACAGAATCTTAGATTCACAAAAATCTCCACAGGCTTATACCCACAGGCTCAGTCTAAGAAGAAGAAATTACAGAGATAAATGCCAATCTTTGAACAGAGATAAATTACCAAACGCATAAATGCAGGATGGAAGAAACCTAACTTTAGTCCACATAAGATGTCTTAGAGTTTAAGTTGGTCTCAAGTTCTGTGTGCACCAGCAGTGACAGCTGCCAATGTATCCTGGGAGCACAGGATGCAGAATAGAGGTCATATGTCCAGA... | AACAATATTTTCCTTGCTGGTGGCACAAAGCCAGGTGAAATAACTAACACATCAGCTGACAGAATCTTAGATTCACAAAAATCTCCACAGGCTTATACCCACAGGCTCAGTCTAAGAAGAAGAAATTACAGAGATAAATGCCAATCTTTGAACAGAGATAAATTACCAAACGCATAAATGCAGGATGGAAGAAACCTAACTTTAGTCCACATAAGATGTCTTAGAGTTTAAGTTGGTCTCAAGTTCTGTGTGCACCAGCAGTGACAGCTGCCAATGTATCCTGGGAGCACAGGATGCAGAATAGAGGTCATATGTCCAGA... |
Task1_train_34411 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | ATGTGCCATGTTGGTGTGCTGCACCCATTAACTGATCATTTACGTTAGGTATATCTCCTAATGCTATCCCTCCTCCCTCCCCCCATCCTATGACAGGCCCCAGTGTGTGATGTTCCCCACCCTGTGTCCATGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGATTTTCTGTCCTTGTGACAGTGAGCAAATCCATCTTTTAAAGAAAGCAAATATTTGTAACCCACCACCTGATATAGAAACAAACATGTTCCACAGGAATCGTTGAACTTTGAGTAATGTGTCCTATAATTCAGCCCTTG... | ATGTGCCATGTTGGTGTGCTGCACCCATTAACTGATCATTTACGTTAGGTATATCTCCTAATGCTATCCCTCCTCCCTCCCCCCATCCTATGACAGGCCCCAGTGTGTGATGTTCCCCACCCTGTGTCCATGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGATTTTCTGTCCTTGTGACAGTGAGCAAATCCATCTTTTAAAGAAAGCAAATATTTGTAACCCACCACCTGATATAGAAACAAACATGTTCCACAGGAATCGTTGAACTTTGAGTAATGTGTCCTATAATTCAGCCCTTG... |
Task1_train_34412 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCGTGTGCAAGTTGGGGGTAGAAGCTAGTAGAGCCAAATTACTCCAGCGTAATAGAGGGGAGAAGAATTTGGAGTTCTCAGGATAATAAGAGAGAATGGGATGGGCTGGATAGGTAGGGAAGATGAAGAATAGAGATGGGAGAGAAAGTAAAACTGATGGGTGACCAAGGAGAGATTGTTTTGAAATATGCTCCTCCCAGGACCTCCAAGTCATTAAATGTTCCCTGTGAGTGGATTTCTTGTGGAAACAACCAAATGAAAGAATTGAGTTTCATATAGGTGGCATGTCATGACAGTGATGTGTTGGTACACCTGCTTTT... | GCGTGTGCAAGTTGGGGGTAGAAGCTAGTAGAGCCAAATTACTCCAGCGTAATAGAGGGGAGAAGAATTTGGAGTTCTCAGGATAATAAGAGAGAATGGGATGGGCTGGATAGGTAGGGAAGATGAAGAATAGAGATGGGAGAGAAAGTAAAACTGATGGGTGACCAAGGAGAGATTGTTTTGAAATATGCTCCTCCCAGGACCTCCAAGTCATTAAATGTTCCCTGTGAGTGGATTTCTTGTGGAAACAACCAAATGAAAGAATTGAGTTTCATATAGGTGGCATGTCATGACAGTGATGTGTTGGTACACCTGCTTTT... |
Task1_train_34413 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTGGGCCAAATACTCACATCACTCATGTTGAGGGCGTTGACTTTGGCTTGAATAAACTGAGGCAATTCAGGGTCAATAGTATACTTGTGCTTCAGTTTCTCTCCCTCTACCTTGTAGTTCAACTAAAAACAAAGGAGACAGCATGCACATATCATTAGCTGACATAATATAAATTTCATCAAGCAGAGACTCCTTTAAAACGGAAGGCTATCATTTGTGTTTTCCATTTACGAGACAAATACCTACTCTGTCATAAGGGAGGGGCCCTGGTAGATGCATTTATGTTCCCATTCTACCAGTATTTATTGGACAGCACTGTG... | CTGGGCCAAATACTCACATCACTCATGTTGAGGGCGTTGACTTTGGCTTGAATAAACTGAGGCAATTCAGGGTCAATAGTATACTTGTGCTTCAGTTTCTCTCCCTCTACCTTGTAGTTCAACTAAAAACAAAGGAGACAGCATGCACATATCATTAGCTGACATAATATAAATTTCATCAAGCAGAGACTCCTTTAAAACGGAAGGCTATCATTTGTGTTTTCCATTTACGAGACAAATACCTACTCTGTCATAAGGGAGGGGCCCTGGTAGATGCATTTATGTTCCCATTCTACCAGTATTTATTGGACAGCACTGTG... |
Task1_train_34414 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTGACTTTGGCTTGAATAAACTGAGGCAATTCAGGGTCAATAGTATACTTGTGCTTCAGTTTCTCTCCCTCTACCTTGTAGTTCAACTAAAAACAAAGGAGACAGCATGCACATATCATTAGCTGACATAATATAAATTTCATCAAGCAGAGACTCCTTTAAAACGGAAGGCTATCATTTGTGTTTTCCATTTACGAGACAAATACCTACTCTGTCATAAGGGAGGGGCCCTGGTAGATGCATTTATGTTCCCATTCTACCAGTATTTATTGGACAGCACTGTGGGCCAGGCAGGGTGGTAAGTTCTGTGTTTAAAGAGG... | TTGACTTTGGCTTGAATAAACTGAGGCAATTCAGGGTCAATAGTATACTTGTGCTTCAGTTTCTCTCCCTCTACCTTGTAGTTCAACTAAAAACAAAGGAGACAGCATGCACATATCATTAGCTGACATAATATAAATTTCATCAAGCAGAGACTCCTTTAAAACGGAAGGCTATCATTTGTGTTTTCCATTTACGAGACAAATACCTACTCTGTCATAAGGGAGGGGCCCTGGTAGATGCATTTATGTTCCCATTCTACCAGTATTTATTGGACAGCACTGTGGGCCAGGCAGGGTGGTAAGTTCTGTGTTTAAAGAGG... |
Task1_train_34415 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | CAGGGGTATGGTAGCTGGTTTTGGTGTTCTCATAGTTCTTCTTGTATTCACGATCAGACTGCAGCTTTGCCACATTCATATAGTGGACCAGCTTGGGATCATCCTGGAGGCTTCTGAAACCCACATGCTTTCCCTTTGACTTCTCATAAGCTTCCTTGTATTTATACTGTGGAGGCAGAATTGGGTTAGCAAAGTCCTAGGCATTGATAGCATTAGCGCTGCAATTACATTCACATATAAAGACACTCAGAGCTTTGTGACTTTCTCAAGAGTGTACAAAAAATGCAAACCACAACCCCCTCCAAAAAGTTCAGTGAAAA... | CAGGGGTATGGTAGCTGGTTTTGGTGTTCTCATAGTTCTTCTTGTATTCACGATCAGACTGCAGCTTTGCCACATTCATATAGTGGACCAGCTTGGGATCATCCTGGAGGCTTCTGAAACCCACATGCTTTCCCTTTGACTTCTCATAAGCTTCCTTGTATTTATACTGTGGAGGCAGAATTGGGTTAGCAAAGTCCTAGGCATTGATAGCATTAGCGCTGCAATTACATTCACATATAAAGACACTCAGAGCTTTGTGACTTTCTCAAGAGTGTACAAAAAATGCAAACCACAACCCCCTCCAAAAAGTTCAGTGAAAA... |
Task1_train_34416 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGTGTAATGATGGAGAGAATGCTTATAGTTGACATTGCTGACCACATCCTGGGCTTTCTTAGCCGCCACGACATTGAACATATCATGGGGCGTGTTGTATTTGGACTTTGTCTTCTCATAGTCTTTTTTATACTCCCGATCTGATTGTATCTTGGCCACGTTCATATAATGAACCAGTTTAGGGTCATCTTGAAGACTTTGGAAGCCAACCATTTTCCCTTTAGCCTTTTCATAGTCTTTTTTGTACTGAACCTATTGTAAACAAAGGTGGGCATAATTTAAAATGTAGTTTTGAGGGCTTTACTAAACAATGAGGCCAT... | GGTGTAATGATGGAGAGAATGCTTATAGTTGACATTGCTGACCACATCCTGGGCTTTCTTAGCCGCCACGACATTGAACATATCATGGGGCGTGTTGTATTTGGACTTTGTCTTCTCATAGTCTTTTTTATACTCCCGATCTGATTGTATCTTGGCCACGTTCATATAATGAACCAGTTTAGGGTCATCTTGAAGACTTTGGAAGCCAACCATTTTCCCTTTAGCCTTTTCATAGTCTTTTTTGTACTGAACCTATTGTAAACAAAGGTGGGCATAATTTAAAATGTAGTTTTGAGGGCTTTACTAAACAATGAGGCCAT... |
Task1_train_34417 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGTTTCTCAACAACATATTTTTGTTTACATGTCAATGTCTTTGTACATTCCTGCCTGCCTTGAAGAACCAGCTCAAATATAACTTCTGAGAAGTCTTCTCACACATCTCTTAACCCCTACTCTTCTTTATACCCCTAGTTCCTTGTTCATAATTCCACTGTCACAGGTATTCTAACCATCTGTCTCTTCTGTCTCTTTGCCCATGGGTAAGATACTGTGTGTGGGTTATGTCTTTATTTCCTAAGTCTAGCACAATGCATGGCACATAACAAGTGTTCAATAAACATTTGATGAAGGAATCTACAAATGTGCATTAACAA... | TGTTTCTCAACAACATATTTTTGTTTACATGTCAATGTCTTTGTACATTCCTGCCTGCCTTGAAGAACCAGCTCAAATATAACTTCTGAGAAGTCTTCTCACACATCTCTTAACCCCTACTCTTCTTTATACCCCTAGTTCCTTGTTCATAATTCCACTGTCACAGGTATTCTAACCATCTGTCTCTTCTGTCTCTTTGCCCATGGGTAAGATACTGTGTGTGGGTTATGTCTTTATTTCCTAAGTCTAGCACAATGCATGGCACATAACAAGTGTTCAATAAACATTTGATGAAGGAATCTACAAATGTGCATTAACAA... |
Task1_train_34418 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCTGGTCCCTAATAATCTTGGAGCTGCACTTTCTGAGAACTGAGGGCTGATCAAGATGATCCTGTATTGTGACAGCTTTCTTTTCAAAATTTTACAGTTATCTGAAAAACTGCAAGACACAGAGAATGAAGCCATGTCCAAGATTGTGGAACTGGAAAAGCAACTCATGCAGAGGAACAAGGAGCTGGATGTCGTTCGGGTAAGTGTAATGATGACAACTGCCCAGATGGGCACGGTAGGGAATGTACTCCAGCTTTCGTCCAGTGGAACGCAGAGTACCTTCATTTCAGAGGAATGCATTGATGCAGCATATTTATTGG... | CCTGGTCCCTAATAATCTTGGAGCTGCACTTTCTGAGAACTGAGGGCTGATCAAGATGATCCTGTATTGTGACAGCTTTCTTTTCAAAATTTTACAGTTATCTGAAAAACTGCAAGACACAGAGAATGAAGCCATGTCCAAGATTGTGGAACTGGAAAAGCAACTCATGCAGAGGAACAAGGAGCTGGATGTCGTTCGGGTAAGTGTAATGATGACAACTGCCCAGATGGGCACGGTAGGGAATGTACTCCAGCTTTCGTCCAGTGGAACGCAGAGTACCTTCATTTCAGAGGAATGCATTGATGCAGCATATTTATTGG... |
Task1_train_34419 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACAAAGAGGAAGATATTTCAGGAATAAAATTCGCTCTAAACCAAAACAATAGCTATTTTCAGATTCTATTTATTTACATGGTCTACCAAAATCAGTTATGTTGCTGTATCAGATAATATTTACTTAGACCATCAACTTCAATTGGCATTCTTGAAAAAATAATCATTAAAAATAAAAGCCTGGATCCACACTTTACTTTTAAATAATAAAGAAAAAAATTCTTAGTTTTGAGGTCATCAGTAAATTTCTCAGAAGACTTTTTCATTATTTAAATTTCTCAGAAGACTTTTCCATTATTCAAATTTCCGTTACAGTCATGA... | ACAAAGAGGAAGATATTTCAGGAATAAAATTCGCTCTAAACCAAAACAATAGCTATTTTCAGATTCTATTTATTTACATGGTCTACCAAAATCAGTTATGTTGCTGTATCAGATAATATTTACTTAGACCATCAACTTCAATTGGCATTCTTGAAAAAATAATCATTAAAAATAAAAGCCTGGATCCACACTTTACTTTTAAATAATAAAGAAAAAAATTCTTAGTTTTGAGGTCATCAGTAAATTTCTCAGAAGACTTTTTCATTATTTAAATTTCTCAGAAGACTTTTCCATTATTCAAATTTCCGTTACAGTCATGA... |
Task1_train_34420 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GCTCCGCCGGCGGCCACTGCCGCTACACATACCAACAAGAAGCGATCTGAGTGGCTGGCGCCCACTGGGGCTAAAGGTTAAAGGCTGCCCTGCGCTACGGGGCGGGATCAGCGGGGCCAACAGGCTGACGGGCTTCCCCGCTGTCCAATCAGAATGCGCCGCCGACACGCAGCTCTGCGGCGATTCGCCCCCAGCCTCAGCCTCACTCGGCGTCGCCTGCATGGGGGGGGGGGAGGAGGAGGACGGAGGAAGTTTCTGCGCCGAGTCCTCCGTCGGGAAAACTCTACCAACTTCCCCAGGGGAAGGGAAGACAACAGTGT... | GCTCCGCCGGCGGCCACTGCCGCTACACATACCAACAAGAAGCGATCTGAGTGGCTGGCGCCCACTGGGGCTAAAGGTTAAAGGCTGCCCTGCGCTACGGGGCGGGATCAGCGGGGCCAACAGGCTGACGGGCTTCCCCGCTGTCCAATCAGAATGCGCCGCCGACACGCAGCTCTGCGGCGATTCGCCCCCAGCCTCAGCCTCACTCGGCGTCGCCTGCATGGGGGGGGGGGAGGAGGAGGACGGAGGAAGTTTCTGCGCCGAGTCCTCCGTCGGGAAAACTCTACCAACTTCCCCAGGGGAAGGGAAGACAACAGTGT... |
Task1_train_34421 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | AATATATATATATATATATATATATATATATATATATATATATATTTAATACAATATCAGCCCAAATGTCATCTCCACCTCCTCTCTCATCAATTGACCAGAGTTTTGGGGATCTTGTTTCAAGTGGTTCTAATGAAAAGCCTGTGGCGGAACTGCTACCCTACCAGTCAACCAGCATCACTCAAAATCTGGTCCAAGTCCTGGTGTGGTCCTGAAACTGTTGCTTGCTGGTTTAAGACGAGATAAGTACTGAAACTGAGAGTAAGTGTATCTTAATCTGTTCAGGCTACTATAGAAGAATAACATAGACTAAGTGACTC... | AATATATATATATATATATATATATATATATATATATATATATATTTAATACAATATCAGCCCAAATGTCATCTCCACCTCCTCTCTCATCAATTGACCAGAGTTTTGGGGATCTTGTTTCAAGTGGTTCTAATGAAAAGCCTGTGGCGGAACTGCTACCCTACCAGTCAACCAGCATCACTCAAAATCTGGTCCAAGTCCTGGTGTGGTCCTGAAACTGTTGCTTGCTGGTTTAAGACGAGATAAGTACTGAAACTGAGAGTAAGTGTATCTTAATCTGTTCAGGCTACTATAGAAGAATAACATAGACTAAGTGACTC... |
Task1_train_34422 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TCAAATAATAAGAATAAATTAACTTTATCTTGAGCTCAAGTTCTTAAACTCACCAATCAATGATTTGTGAGTCATTCTTTTGTTTGTTGGTGGGTTGGTTTCTTTGTGTTTTCTTTTATTTGTTTGTATTTTAAGACATGGATTCTTGGGCCCTCAGCAAACCTTGTAAATTGATTTTCTGGGGCTGAGGATTGGATATTTATGTTTTTCTAAGGCTTTGTCAATTATTATGATAAACAACCATCTAGGAAACCATTGAAATTATGAAGCACAGCTGGATTTGTCTACCATTTCTTAAGTACCCCCTATGTGTCAGATAT... | TCAAATAATAAGAATAAATTAACTTTATCTTGAGCTCAAGTTCTTAAACTCACCAATCAATGATTTGTGAGTCATTCTTTTGTTTGTTGGTGGGTTGGTTTCTTTGTGTTTTCTTTTATTTGTTTGTATTTTAAGACATGGATTCTTGGGCCCTCAGCAAACCTTGTAAATTGATTTTCTGGGGCTGAGGATTGGATATTTATGTTTTTCTAAGGCTTTGTCAATTATTATGATAAACAACCATCTAGGAAACCATTGAAATTATGAAGCACAGCTGGATTTGTCTACCATTTCTTAAGTACCCCCTATGTGTCAGATAT... |
Task1_train_34423 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | TCACATCCCTATTCCCATTCCCAAATTAGACTTTAAAATCCCTGAGGGCAGGACCTATCTATCTTTGTATTCCCTCTTGTACCCGATATTGTGGCAAGCAAGATATGGGTGCTCTATGATTATTTAATAAGTGGATGAGAGCATTAACGAGTATGGAAGTACACGCAAACTCCATAGCTGTCAGTTTTTTGCCTTCCTTATTTCAACTCAGTAAAATGAAGATAGATTCAGTAACATATTTCCATAGTGAAATGAAGCATAATCACTAAATTGTACTCTATGAGAAAATACAGAAGTATATCCTTCAGAACGCTATTACC... | TCACATCCCTATTCCCATTCCCAAATTAGACTTTAAAATCCCTGAGGGCAGGACCTATCTATCTTTGTATTCCCTCTTGTACCCGATATTGTGGCAAGCAAGATATGGGTGCTCTATGATTATTTAATAAGTGGATGAGAGCATTAACGAGTATGGAAGTACACGCAAACTCCATAGCTGTCAGTTTTTTGCCTTCCTTATTTCAACTCAGTAAAATGAAGATAGATTCAGTAACATATTTCCATAGTGAAATGAAGCATAATCACTAAATTGTACTCTATGAGAAAATACAGAAGTATATCCTTCAGAACGCTATTACC... |
Task1_train_34424 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | CAATACAGTCAATCAAAAAGCATTGCTGAGAAACAACCTACCATAAGAGCAGGATCGAGTCTTGAGAAGATTGAAAGGTGGGGAGAATAATTTAAGACTGCCCAGAAGGCATTAACTAGTATTCTACTTTCATCAACTTTTATAGATTCCACAAGATTATTCTGAACTTCATCCAAATGACAATTACTTGCCTAAATGTCTGACCGAGTTGTTACATGGGGTCCATAAATCTTAGATGGCATTACCTGGCACTGTTAGTGATCAAGATCACTGGTTGACTGAATCTGCACCGGAAACAGACATGTTAATCAACCTAGTTA... | CAATACAGTCAATCAAAAAGCATTGCTGAGAAACAACCTACCATAAGAGCAGGATCGAGTCTTGAGAAGATTGAAAGGTGGGGAGAATAATTTAAGACTGCCCAGAAGGCATTAACTAGTATTCTACTTTCATCAACTTTTATAGATTCCACAAGATTATTCTGAACTTCATCCAAATGACAATTACTTGCCTAAATGTCTGACCGAGTTGTTACATGGGGTCCATAAATCTTAGATGGCATTACCTGGCACTGTTAGTGATCAAGATCACTGGTTGACTGAATCTGCACCGGAAACAGACATGTTAATCAACCTAGTTA... |
Task1_train_34425 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ACACATCTGAGCCTTATGATGTAGTGATTCTGCTCCTAAGTATACTATCTATCCAATAGAAATGAATGTATATGTCCAACAAAAGACATGTTCAAGAATGTTGATAGTGCCATTATCATAATAGCAAAAACCTGAAAACGGCTCAAATTTCTGTTAGCAGGAAAATATATACATATACTATGAAATACTAAACAGCAATAAAGAAGAACAAATAGCTGTAACATGCCACAAAGATGAAACAGATATGATGAATCCAAGAAGTACAAAGGACTATATACTGTATATATCATTTGATTTATATGAAGTTCAGGAACAGACAA... | ACACATCTGAGCCTTATGATGTAGTGATTCTGCTCCTAAGTATACTATCTATCCAATAGAAATGAATGTATATGTCCAACAAAAGACATGTTCAAGAATGTTGATAGTGCCATTATCATAATAGCAAAAACCTGAAAACGGCTCAAATTTCTGTTAGCAGGAAAATATATACATATACTATGAAATACTAAACAGCAATAAAGAAGAACAAATAGCTGTAACATGCCACAAAGATGAAACAGATATGATGAATCCAAGAAGTACAAAGGACTATATACTGTATATATCATTTGATTTATATGAAGTTCAGGAACAGACAA... |
Task1_train_34426 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | ATATCTGACATAGCTAAATGGAGCATCAGACAATTATGTCTCATCTATATGGTTAATTCATCCAAATGTTAGGAAATTAAAGCCACAATCTCATCTGAGTCTCAAACAAGCAATTAAACTTGTCTTCATGTTACTGATGAAATACAGCCCAAATAGAATCTAAATAGCTTCACAAAAACACTGAATAAAGAAAGAGGTTCAATTGTAGTCAAATTGTTTTTAAAATGTGTTTCAGTAAAAGAGATCATCCTTTAAAGCTGTGCTGTCCAAGATGTTAGCCCCTAGCCACATGTGGCTTAAAAATGTGGCAGTCCAAATTA... | ATATCTGACATAGCTAAATGGAGCATCAGACAATTATGTCTCATCTATATGGTTAATTCATCCAAATGTTAGGAAATTAAAGCCACAATCTCATCTGAGTCTCAAACAAGCAATTAAACTTGTCTTCATGTTACTGATGAAATACAGCCCAAATAGAATCTAAATAGCTTCACAAAAACACTGAATAAAGAAAGAGGTTCAATTGTAGTCAAATTGTTTTTAAAATGTGTTTCAGTAAAAGAGATCATCCTTTAAAGCTGTGCTGTCCAAGATGTTAGCCCCTAGCCACATGTGGCTTAAAAATGTGGCAGTCCAAATTA... |
Task1_train_34427 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | CACCATGCAGAAGTGGATAATCATTCTTGGGAGAAAACCAGAAGTCTATTTCCTAAAAATGAAATTTAACATATAGAAGAAATTTTTTTAAAATTTAGAAAACATACTCTGTGTTGATCATAGGATAAAATTACAGTCAATTACAAGTAACATAATTCCATGGGTACATTTTCCATTGTATCAATTACTGCAGAGCAGCTTCACATCTTGAAAAGAAAAGTTGTGGTTACTGAAAATTCATATTTGAAAACTATTTCTTACCTGTGTAGTGAAGAGCTCAATAAGAGACATTTTCAACATGTCTTAACCTTATAAAAATC... | CACCATGCAGAAGTGGATAATCATTCTTGGGAGAAAACCAGAAGTCTATTTCCTAAAAATGAAATTTAACATATAGAAGAAATTTTTTTAAAATTTAGAAAACATACTCTGTGTTGATCATAGGATAAAATTACAGTCAATTACAAGTAACATAATTCCATGGGTACATTTTCCATTGTATCAATTACTGCAGAGCAGCTTCACATCTTGAAAAGAAAAGTTGTGGTTACTGAAAATTCATATTTGAAAACTATTTCTTACCTGTGTAGTGAAGAGCTCAATAAGAGACATTTTCAACATGTCTTAACCTTATAAAAATC... |
Task1_train_34428 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | GCATTCCTATACACCAATAATAGACAGAGAGCCAAATCATGAGTGAACTCCCATTCATAATTGCTACAAAGAGAATAAAATACCTAGGAATACAACTTACAAGTGATGTGAAGGACCTCTTCAAGGAGAACTACAAACCACTACTCAAGGAAGTAAGAGAGGACACAAACAAATGGAAAAATATTCCATGCTCATGGATAGGAAGAATGAATATCGTGAAAATGGCCATACTGCCCAAAGTAATTTATAGATTCAATGCTATCCCTATCAAGCTACCACTGACTTTCTTCACAGAATTGGAAAAAACTACTTTAAACTTT... | GCATTCCTATACACCAATAATAGACAGAGAGCCAAATCATGAGTGAACTCCCATTCATAATTGCTACAAAGAGAATAAAATACCTAGGAATACAACTTACAAGTGATGTGAAGGACCTCTTCAAGGAGAACTACAAACCACTACTCAAGGAAGTAAGAGAGGACACAAACAAATGGAAAAATATTCCATGCTCATGGATAGGAAGAATGAATATCGTGAAAATGGCCATACTGCCCAAAGTAATTTATAGATTCAATGCTATCCCTATCAAGCTACCACTGACTTTCTTCACAGAATTGGAAAAAACTACTTTAAACTTT... |
Task1_train_34429 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | CTTTCTGAGGAGTGCTTCAGAGACTATTAATTTTGAAATGGTTTCCACAGATCAGTTGATGAGTAATTCAAAAGGATCTGAGTAGAGGATGCTCCAGGCACCTCCATAAGAGTTAAACCATATCAGAAAGAGAATGGAAATAGACTGTGGCACTTCTTTGACTCTTTTCTATAAAATTATTTTTAAATCACTTTTAAAGATTGCTTCCTAATTTCTGGGAAGACATTTTTTGAGGATTTGCCTCCCTCCACTTTAGAATGAAATACTGATTCGCTCCATTAGCAGCAAGTCATTTGTTATTTCTGATATCAGAAACTAAC... | CTTTCTGAGGAGTGCTTCAGAGACTATTAATTTTGAAATGGTTTCCACAGATCAGTTGATGAGTAATTCAAAAGGATCTGAGTAGAGGATGCTCCAGGCACCTCCATAAGAGTTAAACCATATCAGAAAGAGAATGGAAATAGACTGTGGCACTTCTTTGACTCTTTTCTATAAAATTATTTTTAAATCACTTTTAAAGATTGCTTCCTAATTTCTGGGAAGACATTTTTTGAGGATTTGCCTCCCTCCACTTTAGAATGAAATACTGATTCGCTCCATTAGCAGCAAGTCATTTGTTATTTCTGATATCAGAAACTAAC... |
Task1_train_34430 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CAGAGACTATTAATTTTGAAATGGTTTCCACAGATCAGTTGATGAGTAATTCAAAAGGATCTGAGTAGAGGATGCTCCAGGCACCTCCATAAGAGTTAAACCATATCAGAAAGAGAATGGAAATAGACTGTGGCACTTCTTTGACTCTTTTCTATAAAATTATTTTTAAATCACTTTTAAAGATTGCTTCCTAATTTCTGGGAAGACATTTTTTGAGGATTTGCCTCCCTCCACTTTAGAATGAAATACTGATTCGCTCCATTAGCAGCAAGTCATTTGTTATTTCTGATATCAGAAACTAACCATCACATGACAAAAGG... | CAGAGACTATTAATTTTGAAATGGTTTCCACAGATCAGTTGATGAGTAATTCAAAAGGATCTGAGTAGAGGATGCTCCAGGCACCTCCATAAGAGTTAAACCATATCAGAAAGAGAATGGAAATAGACTGTGGCACTTCTTTGACTCTTTTCTATAAAATTATTTTTAAATCACTTTTAAAGATTGCTTCCTAATTTCTGGGAAGACATTTTTTGAGGATTTGCCTCCCTCCACTTTAGAATGAAATACTGATTCGCTCCATTAGCAGCAAGTCATTTGTTATTTCTGATATCAGAAACTAACCATCACATGACAAAAGG... |
Task1_train_34431 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ACTACAGTCGCTCGCCACCATGCCCGGCTAATTTTTCATATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCGCCTGACCTCATGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGGGCCACCGAGCCCGGCCTCCTTTCCTTTTTCTTTTCCTACCTCCACCCATCATCTCTTTCACACTTAAGAACAACAATCAACATGTGGCTTTCTTTGTTTCAGTCCCAACTTGTCCTCTTACCCTCCCTTACCTTGGCTAATTGCCCAAATTTCTGTTATATCAGAGTTTTTTT... | ACTACAGTCGCTCGCCACCATGCCCGGCTAATTTTTCATATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCGCCTGACCTCATGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGGGCCACCGAGCCCGGCCTCCTTTCCTTTTTCTTTTCCTACCTCCACCCATCATCTCTTTCACACTTAAGAACAACAATCAACATGTGGCTTTCTTTGTTTCAGTCCCAACTTGTCCTCTTACCCTCCCTTACCTTGGCTAATTGCCCAAATTTCTGTTATATCAGAGTTTTTTT... |
Task1_train_34432 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCTCTGTTGAAAACTTTTGGAAGCTGGGCGCGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCGAATCACAAGGTCAGGTGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTCCTAAAAAGAGAAAAAAATGAGCCGGGCGTAGTGGCGGGTGCCTGTAATCTCAGCTACTCGACAGGCTGAGGCAAGAGAATAGCTTGAACCTGGGATGCGGAGGTTGCAGTGAGCCGAGATCACTCCACTGCACTCCAGCCTGGGCAAGAGAACGAGACTCCGTCTCAAAAACAAAAACAAAAA... | GCTCTGTTGAAAACTTTTGGAAGCTGGGCGCGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCGAATCACAAGGTCAGGTGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTCCTAAAAAGAGAAAAAAATGAGCCGGGCGTAGTGGCGGGTGCCTGTAATCTCAGCTACTCGACAGGCTGAGGCAAGAGAATAGCTTGAACCTGGGATGCGGAGGTTGCAGTGAGCCGAGATCACTCCACTGCACTCCAGCCTGGGCAAGAGAACGAGACTCCGTCTCAAAAACAAAAACAAAAA... |
Task1_train_34433 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTCCTAAAAAGAGAAAAAAATGAGCCGGGCGTAGTGGCGGGTGCCTGTAATCTCAGCTACTCGACAGGCTGAGGCAAGAGAATAGCTTGAACCTGGGATGCGGAGGTTGCAGTGAGCCGAGATCACTCCACTGCACTCCAGCCTGGGCAAGAGAACGAGACTCCGTCTCAAAAACAAAAACAAAAACAAAAAAGAACCCACAACATTTTGAGGGTTGGGAGACCATCAGGTTTAGTGCCCGGGACTTAGAGTCTGGCCATTAATTTTCAACACCACCTTTCC... | TTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTCCTAAAAAGAGAAAAAAATGAGCCGGGCGTAGTGGCGGGTGCCTGTAATCTCAGCTACTCGACAGGCTGAGGCAAGAGAATAGCTTGAACCTGGGATGCGGAGGTTGCAGTGAGCCGAGATCACTCCACTGCACTCCAGCCTGGGCAAGAGAACGAGACTCCGTCTCAAAAACAAAAACAAAAACAAAAAAGAACCCACAACATTTTGAGGGTTGGGAGACCATCAGGTTTAGTGCCCGGGACTTAGAGTCTGGCCATTAATTTTCAACACCACCTTTCC... |
Task1_train_34434 | This genomic variant is located on Chromosome 2. Can you determine its pathogenicity and name any linked disease? | Benign | AATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATCGCTTGAACCCAGGAGGTGGACGTTGCAGTGAGTCGAGATCGTGCCACTGCACTCCAGCCTGGGCAACACAGCAAGACTGTCTCAAAAAAAAAAAAAAAAAAAAAAAGTAAGGCATGTACCTGTCCTATATGTCTCATATAAGGCATATGTCCTATATGGAGGGGGTGACTCTACTTCCTCTTGACTCCTAACACAAAAAACAAGCACAGTGATACCACTTGAAACTTGATGGTCTGGTTTGTATCCCCTTTGAGCCTTGTACACAAAAATCTGCAGAATTTAGT... | AATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATCGCTTGAACCCAGGAGGTGGACGTTGCAGTGAGTCGAGATCGTGCCACTGCACTCCAGCCTGGGCAACACAGCAAGACTGTCTCAAAAAAAAAAAAAAAAAAAAAAAGTAAGGCATGTACCTGTCCTATATGTCTCATATAAGGCATATGTCCTATATGGAGGGGGTGACTCTACTTCCTCTTGACTCCTAACACAAAAAACAAGCACAGTGATACCACTTGAAACTTGATGGTCTGGTTTGTATCCCCTTTGAGCCTTGTACACAAAAATCTGCAGAATTTAGT... |
Task1_train_34435 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | AATGAATTAAGGGTTTCCCTCTATCTCAATTTGTCGCGATGCCGAAGAAAAACAAATGTAAGCTGTGCCCCTTTATTCCAACCCAGTCTTCCAGCAACAGAGCCCTTCTCCAGCAGTGAAGGCCAGCCCTTCTCCAGACCAGATCCTGGGCCCTCCTGTCCAATTTGCTTGCACATTTACATGAACCTGGCATGTGGGAAACAGCTCCTATCCGTGACTATCGTTTGGTCACGGCTGCTACGCTCCTCGCATGATGTTGAAGGAATGCACTTGGGTTTCGTTTCCTTGGCCTCAGTAATGAGAAGCAAATGCAGTCTGCT... | AATGAATTAAGGGTTTCCCTCTATCTCAATTTGTCGCGATGCCGAAGAAAAACAAATGTAAGCTGTGCCCCTTTATTCCAACCCAGTCTTCCAGCAACAGAGCCCTTCTCCAGCAGTGAAGGCCAGCCCTTCTCCAGACCAGATCCTGGGCCCTCCTGTCCAATTTGCTTGCACATTTACATGAACCTGGCATGTGGGAAACAGCTCCTATCCGTGACTATCGTTTGGTCACGGCTGCTACGCTCCTCGCATGATGTTGAAGGAATGCACTTGGGTTTCGTTTCCTTGGCCTCAGTAATGAGAAGCAAATGCAGTCTGCT... |
Task1_train_34436 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTGGCATGTGGGAAACAGCTCCTATCCGTGACTATCGTTTGGTCACGGCTGCTACGCTCCTCGCATGATGTTGAAGGAATGCACTTGGGTTTCGTTTCCTTGGCCTCAGTAATGAGAAGCAAATGCAGTCTGCTCCTCTGCAGCTTCCCAACACTGTTGCTGCTGGCACTGCCGTCCCCGGATTCAGGAGAGTCCAACCCAAGCCTATTGTGGTGGGCCTGCCTTCTGTGTTAGGTTTGCTCAGAGGGTCTGCCAGTAACTAATTTGTAACCGGTCGTGGGGAACTCATAGTCGATTTGTAACTAGTAGATCTGTTTCAG... | CTGGCATGTGGGAAACAGCTCCTATCCGTGACTATCGTTTGGTCACGGCTGCTACGCTCCTCGCATGATGTTGAAGGAATGCACTTGGGTTTCGTTTCCTTGGCCTCAGTAATGAGAAGCAAATGCAGTCTGCTCCTCTGCAGCTTCCCAACACTGTTGCTGCTGGCACTGCCGTCCCCGGATTCAGGAGAGTCCAACCCAAGCCTATTGTGGTGGGCCTGCCTTCTGTGTTAGGTTTGCTCAGAGGGTCTGCCAGTAACTAATTTGTAACCGGTCGTGGGGAACTCATAGTCGATTTGTAACTAGTAGATCTGTTTCAG... |
Task1_train_34437 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CCCATCAAGCTACCATTGACTTTTTTCACAGAATTAGAAAAAACTACTTTAAATTTCATATGGAACTAAAAAAGAGCCTGTATAGCCAACACAATCCTAAGCAAAAAGAACAAAGCTAGAGGCATCACGCTACCTGACTTCAAACTATACTACGAGGCTACAGTAACCAAAACAGCATGGTGCTGGTACCAAAACAGATATATAGACCAATGGAACAGAACAGAGGCCTCAGAAATAATGCCACACATCTACAACCCTCTGATCTTTGACAAACCTGAGAAAAACAAGCAACAGGGAAAGGATTCCCTATTTAATAAATG... | CCCATCAAGCTACCATTGACTTTTTTCACAGAATTAGAAAAAACTACTTTAAATTTCATATGGAACTAAAAAAGAGCCTGTATAGCCAACACAATCCTAAGCAAAAAGAACAAAGCTAGAGGCATCACGCTACCTGACTTCAAACTATACTACGAGGCTACAGTAACCAAAACAGCATGGTGCTGGTACCAAAACAGATATATAGACCAATGGAACAGAACAGAGGCCTCAGAAATAATGCCACACATCTACAACCCTCTGATCTTTGACAAACCTGAGAAAAACAAGCAACAGGGAAAGGATTCCCTATTTAATAAATG... |
Task1_train_34438 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCAGTGAGCCGAGATGCACCACTGCACTCCAGCTTGGGCAACAAAAGTGAAACTCTCTCAAAAAAAAAAAAAAAGAACAAACAAAAGAACTAGTCCATATCTAGGTAACAGTGTTTGCATATTGGAACCAATCAGTACCAATCAATCATTTAAACGCTTCCTTAACTTAGGCAGGTCCCTTCTGTAATTAAAAAATAATAAAACAAAACAGACATAAACCTTTGGACGGCTGTTATTTCATCCTCCAAAGAAATAAATTTGTCATTTGGTCAATCTAGTAAATCAGTTGATATATGTGAGGGATGCTGATCATTATAAGT... | GCAGTGAGCCGAGATGCACCACTGCACTCCAGCTTGGGCAACAAAAGTGAAACTCTCTCAAAAAAAAAAAAAAAGAACAAACAAAAGAACTAGTCCATATCTAGGTAACAGTGTTTGCATATTGGAACCAATCAGTACCAATCAATCATTTAAACGCTTCCTTAACTTAGGCAGGTCCCTTCTGTAATTAAAAAATAATAAAACAAAACAGACATAAACCTTTGGACGGCTGTTATTTCATCCTCCAAAGAAATAAATTTGTCATTTGGTCAATCTAGTAAATCAGTTGATATATGTGAGGGATGCTGATCATTATAAGT... |
Task1_train_34439 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | CCATATATTGACACCAATAAGTTTTTAAAAATAGCCAAAGATTTCTATATTTTATCCCAATTACTCTTTTATAGTACACATATTATCATTTTTAAAATCAGGAGTGATGTGTAAAAAGGAGATGGAGAGAAAATTGAGACCTGTATAGCAGCAAATCTCTTGCTGCTTTAAGATATCCATTTGGGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACTTGAGGTCAGGAGTTTGTGACTAGCCTGGCCAACATGGTGAAACCACATCTCTACTAAAAATACAAAAAAAT... | CCATATATTGACACCAATAAGTTTTTAAAAATAGCCAAAGATTTCTATATTTTATCCCAATTACTCTTTTATAGTACACATATTATCATTTTTAAAATCAGGAGTGATGTGTAAAAAGGAGATGGAGAGAAAATTGAGACCTGTATAGCAGCAAATCTCTTGCTGCTTTAAGATATCCATTTGGGGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACTTGAGGTCAGGAGTTTGTGACTAGCCTGGCCAACATGGTGAAACCACATCTCTACTAAAAATACAAAAAAAT... |
Task1_train_34440 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TAGATGTCCAAAGAATTTTGTACCTTAAATGAATAAGTGAATACTTTATTTTGGCTGGGGGAGCTATCAAATTTTTTTCTATATAGTAGAAGTATCAACATTATTGAACTCCAGATGAGTAATTTTTTAAATGTGTTAACCATCATTCTAGTACAAAAGACATTTGATTTTAATAATATAGTATTTACATTGTGGCTTAGAAATGTTCAAAAGCAACAGTGTAATAAAGCATGATAAAACAATAAAAATATTTAAGATATCACTATCTATATTGTTTTTATCTATTTTGATATTTATTCAGCAATCTTGTATTTCAGTAA... | TAGATGTCCAAAGAATTTTGTACCTTAAATGAATAAGTGAATACTTTATTTTGGCTGGGGGAGCTATCAAATTTTTTTCTATATAGTAGAAGTATCAACATTATTGAACTCCAGATGAGTAATTTTTTAAATGTGTTAACCATCATTCTAGTACAAAAGACATTTGATTTTAATAATATAGTATTTACATTGTGGCTTAGAAATGTTCAAAAGCAACAGTGTAATAAAGCATGATAAAACAATAAAAATATTTAAGATATCACTATCTATATTGTTTTTATCTATTTTGATATTTATTCAGCAATCTTGTATTTCAGTAA... |
Task1_train_34441 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAGCCCAGGAATTCAAGACCAGCTAGGCAACATGGTGAGACCCTGTCTCTACAAAATAAAAATTACCTAGCCATGATGATATGTGCCTGTGGTCCCAGCTACTCTGGAGACTGAGGTGGGAGGATCAAGGCAGCAGTGAGCTGTGATTGTGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGATGCTGTCTCAAAAAAAAACAACAAAAAAATCTGATGGTAAAATGGTTTATACGTCTTTTTGTGTTGTTTATTTGTAATGTCTTTTTTCATTCATCTACCCCGTGAACTTCAGTTACCATCTTTGACTCTTCCCCTG... | GAGCCCAGGAATTCAAGACCAGCTAGGCAACATGGTGAGACCCTGTCTCTACAAAATAAAAATTACCTAGCCATGATGATATGTGCCTGTGGTCCCAGCTACTCTGGAGACTGAGGTGGGAGGATCAAGGCAGCAGTGAGCTGTGATTGTGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGATGCTGTCTCAAAAAAAAACAACAAAAAAATCTGATGGTAAAATGGTTTATACGTCTTTTTGTGTTGTTTATTTGTAATGTCTTTTTTCATTCATCTACCCCGTGAACTTCAGTTACCATCTTTGACTCTTCCCCTG... |
Task1_train_34442 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TTGACCTCAAGACCCACACTTTGTTTTTGGTTTGTTTGTTCTGAGATGGAGTTTTGCTCTTGTTACCCAGGCTGGGGTGCAATGGCACGACGTCAGCTCACTGCAGCCTTCGCCTCCTGGGTTCAAGCGATTCTCCTGTGTCAGCCTCTCAAGTAGCTGGGGTTACAGGCATATGCCACCATGCCCAGCTAATTTTGTGTTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCAACCGCCTCAGCCTCCCAAAGTGTTGAGATTACAGGTATGAGCCACTGCACAC... | TTGACCTCAAGACCCACACTTTGTTTTTGGTTTGTTTGTTCTGAGATGGAGTTTTGCTCTTGTTACCCAGGCTGGGGTGCAATGGCACGACGTCAGCTCACTGCAGCCTTCGCCTCCTGGGTTCAAGCGATTCTCCTGTGTCAGCCTCTCAAGTAGCTGGGGTTACAGGCATATGCCACCATGCCCAGCTAATTTTGTGTTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCAACCGCCTCAGCCTCCCAAAGTGTTGAGATTACAGGTATGAGCCACTGCACAC... |
Task1_train_34443 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCAAAATTATTTTCACAAAAATTATTTGTGAATACATCTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTTGCTCTGTCTCCCAGGCTGGACTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCCGCCTCAGCCTCCTGACTAGCTGGGACTACAGGCGCCCGCCACCATGCCCAGCTATTTTTTTTGCATTTTTAGTAGAGAAGGGGTTTCACCTTGTTAGCCAGGATGATCTCCATCTCCTGACCTCGTGATCCGCACGCCTCGGCCTCCCAAAGTGCTGGGATTACAGG... | TCAAAATTATTTTCACAAAAATTATTTGTGAATACATCTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTTGCTCTGTCTCCCAGGCTGGACTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCCGCCTCAGCCTCCTGACTAGCTGGGACTACAGGCGCCCGCCACCATGCCCAGCTATTTTTTTTGCATTTTTAGTAGAGAAGGGGTTTCACCTTGTTAGCCAGGATGATCTCCATCTCCTGACCTCGTGATCCGCACGCCTCGGCCTCCCAAAGTGCTGGGATTACAGG... |
Task1_train_34444 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAATCCCAGCATTTTGGGAGGCCAAGGCGGGGGGATCACCTGAGGTCAGGAGTTCAAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACCAAAAATACAAAAAATTAGCTGGGCATGGTGGGGCGTGCCTGTAATCCCAGGTACTTGGGAGGCTGAGGCAGGAGAATCGCTGGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATGGCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCCAAAAAAATAAATAAATAAATAAAATAATAAAATAAAATAAAAATTGGAGAAAATAGACAAA... | TAATCCCAGCATTTTGGGAGGCCAAGGCGGGGGGATCACCTGAGGTCAGGAGTTCAAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACCAAAAATACAAAAAATTAGCTGGGCATGGTGGGGCGTGCCTGTAATCCCAGGTACTTGGGAGGCTGAGGCAGGAGAATCGCTGGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATGGCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCCAAAAAAATAAATAAATAAATAAAATAATAAAATAAAATAAAAATTGGAGAAAATAGACAAA... |
Task1_train_34445 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TGAAACCCCGTCTCTACCAAAAATACAAAAAATTAGCTGGGCATGGTGGGGCGTGCCTGTAATCCCAGGTACTTGGGAGGCTGAGGCAGGAGAATCGCTGGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATGGCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCCAAAAAAATAAATAAATAAATAAAATAATAAAATAAAATAAAAATTGGAGAAAATAGACAAATATCCTGTGCAGAAGAATTTCAAGTAATTTATATCGATACTCCCCTCATAGGAAGGTGGAGGATAACTTTCTACCCT... | TGAAACCCCGTCTCTACCAAAAATACAAAAAATTAGCTGGGCATGGTGGGGCGTGCCTGTAATCCCAGGTACTTGGGAGGCTGAGGCAGGAGAATCGCTGGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATGGCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCCAAAAAAATAAATAAATAAATAAAATAATAAAATAAAATAAAAATTGGAGAAAATAGACAAATATCCTGTGCAGAAGAATTTCAAGTAATTTATATCGATACTCCCCTCATAGGAAGGTGGAGGATAACTTTCTACCCT... |
Task1_train_34446 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTGGCTTACTGCATCCTCCACCTCCCAGATTCAAGTGATTCTCATACTTCAGCCTCCCAAGAAGCTGGGATTGCAGGTGCATGCTGCCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGATTCACCACGTTGGCCAGGCTGGTCTCGAACTCCTTGCCTCAAGTGATTTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCCGGCCAAGTCAGCACATTTTAAAAGCAACCCAGTAGTAAAGAAAGGCTCTTGAAATCAATCTTTCCTAAATGCTTAAAATATATTCCCTTTC... | TTGGCTTACTGCATCCTCCACCTCCCAGATTCAAGTGATTCTCATACTTCAGCCTCCCAAGAAGCTGGGATTGCAGGTGCATGCTGCCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGATTCACCACGTTGGCCAGGCTGGTCTCGAACTCCTTGCCTCAAGTGATTTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCCGGCCAAGTCAGCACATTTTAAAAGCAACCCAGTAGTAAAGAAAGGCTCTTGAAATCAATCTTTCCTAAATGCTTAAAATATATTCCCTTTC... |
Task1_train_34447 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTCAAAAAACAAAACAAAAAGCAAATCTGGAAAATATAGAAATTTTCAAAGAAAACATTCTATTCATTTATTTTTTACAGACAGCATCTCACTCTGTTGCCCAAGCTGGAGTGCAGTGGCACTATCTTGTCTCACTGTATCCTTGAACTCCTGGGCTCAAGTGATCCTCCTGACTCAGCCTCCTGAGTAACCAGGACTACAGGTGTGTGCCACCATGCCCAGCTAATTCTTTTTTTTTTTTTTTTAAATAGAGATAGGGTCTCCCTATGCTACCCAGGCTGGTCTCGAACTCCTGGTTTCAAGCAATCCTCTCACCTCAG... | CTCAAAAAACAAAACAAAAAGCAAATCTGGAAAATATAGAAATTTTCAAAGAAAACATTCTATTCATTTATTTTTTACAGACAGCATCTCACTCTGTTGCCCAAGCTGGAGTGCAGTGGCACTATCTTGTCTCACTGTATCCTTGAACTCCTGGGCTCAAGTGATCCTCCTGACTCAGCCTCCTGAGTAACCAGGACTACAGGTGTGTGCCACCATGCCCAGCTAATTCTTTTTTTTTTTTTTTTAAATAGAGATAGGGTCTCCCTATGCTACCCAGGCTGGTCTCGAACTCCTGGTTTCAAGCAATCCTCTCACCTCAG... |
Task1_train_34448 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTGGAAAAACCCCCTTATTGTACACATTTTGTCCCTCTGCACCTCTCCTTTTTTACTTGATTTTTCAATGCAAAGACTTGCCTGACAGAGAAGGATAGAAGAGGGCTGGGTGCTGTGGGGCACAAGGTAGAGAAGCCTGGGCTTACTCCTGTGTCTATAGGTTTTGCCTCATTACGGAGGCATGAACTGCAGTGGTTCTCAGACTTGAATACGCATCAGAACCACCTGGAAAGTTTCTTAAAATACAGATTGCTGGACCCCATCCTGTAGTTTCTGATGTAGCAAATCTGGGGTGGGTCCTGAGAGCTTGCATTTCTAAC... | CTGGAAAAACCCCCTTATTGTACACATTTTGTCCCTCTGCACCTCTCCTTTTTTACTTGATTTTTCAATGCAAAGACTTGCCTGACAGAGAAGGATAGAAGAGGGCTGGGTGCTGTGGGGCACAAGGTAGAGAAGCCTGGGCTTACTCCTGTGTCTATAGGTTTTGCCTCATTACGGAGGCATGAACTGCAGTGGTTCTCAGACTTGAATACGCATCAGAACCACCTGGAAAGTTTCTTAAAATACAGATTGCTGGACCCCATCCTGTAGTTTCTGATGTAGCAAATCTGGGGTGGGTCCTGAGAGCTTGCATTTCTAAC... |
Task1_train_34449 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | AATCCCCACCAGCAAGGAGATCCTCTCCAGATGTGGTCCTTTGACCTTGAACTTCCCAGCCTCCATAACTGTAGGAAATAAATTTCTTTTATTTATAAATTACTCAGTTTCTTTGTATTCTACTATAATCAATAGAAAATGGACTAAGACATCCCCATAATATCCAGATCTGCTTGATATAGGCCTTATAAGTGAGGCAGAATGTGAGCTAAAGCCAATGCAACAACAAAGCCTAAGCAAGTTGGATTCCTGGGGCTCTGGTTTCTGCTAGAACCATGTATGTATGTTAAGCAGATCTGAAAAATCTGGTTTTGCTTCTG... | AATCCCCACCAGCAAGGAGATCCTCTCCAGATGTGGTCCTTTGACCTTGAACTTCCCAGCCTCCATAACTGTAGGAAATAAATTTCTTTTATTTATAAATTACTCAGTTTCTTTGTATTCTACTATAATCAATAGAAAATGGACTAAGACATCCCCATAATATCCAGATCTGCTTGATATAGGCCTTATAAGTGAGGCAGAATGTGAGCTAAAGCCAATGCAACAACAAAGCCTAAGCAAGTTGGATTCCTGGGGCTCTGGTTTCTGCTAGAACCATGTATGTATGTTAAGCAGATCTGAAAAATCTGGTTTTGCTTCTG... |
Task1_train_34450 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | GCGTGGTGGCTCACGCCGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGGACTGCCTCAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTATAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTGGGCCACAAAAGCAAGACTTCAATCAATCCACAGAAGAATGTGTTGAACTTGAAGCAAAGCAAATAATCCAAAC... | GCGTGGTGGCTCACGCCGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGGACTGCCTCAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTATAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTGGGCCACAAAAGCAAGACTTCAATCAATCCACAGAAGAATGTGTTGAACTTGAAGCAAAGCAAATAATCCAAAC... |
Task1_train_34451 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CAGCACTTTGGGAGGCTGAGGTGGGCGGACTGCCTCAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTATAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTGGGCCACAAAAGCAAGACTTCAATCAATCCACAGAAGAATGTGTTGAACTTGAAGCAAAGCAAATAATCCAAACAAGCTAACTTAACTACTCCCATTT... | CAGCACTTTGGGAGGCTGAGGTGGGCGGACTGCCTCAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTATAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTGGGCCACAAAAGCAAGACTTCAATCAATCCACAGAAGAATGTGTTGAACTTGAAGCAAAGCAAATAATCCAAACAAGCTAACTTAACTACTCCCATTT... |
Task1_train_34452 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | ACAGTAGTACATTTAGCTATTTTATGCATTTGGTTTCTTGCATAGTTTCCAAAACATTCTAGAAGACAGCAATACTTTAAATGGAGTCAGCTGGAGTTTAAAAAAGTATTTTAAGAAAACCATCAATTATGTGTGTCTTCTTTTGTCCTCCTGTATACCCAAGAGATCTCATTGGTTAATATTCATCTCTGATTAGGCATTATCAAGGAAAGATTCAAAACTACTGTAATATCAACTCAACTAATCCATCAAAGCTTCAGAAGAATGTTCTTTTCACACCCTCCAACATTTTGTTTCTTCTTAGTCACAGGAGGTAAATG... | ACAGTAGTACATTTAGCTATTTTATGCATTTGGTTTCTTGCATAGTTTCCAAAACATTCTAGAAGACAGCAATACTTTAAATGGAGTCAGCTGGAGTTTAAAAAAGTATTTTAAGAAAACCATCAATTATGTGTGTCTTCTTTTGTCCTCCTGTATACCCAAGAGATCTCATTGGTTAATATTCATCTCTGATTAGGCATTATCAAGGAAAGATTCAAAACTACTGTAATATCAACTCAACTAATCCATCAAAGCTTCAGAAGAATGTTCTTTTCACACCCTCCAACATTTTGTTTCTTCTTAGTCACAGGAGGTAAATG... |
Task1_train_34453 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | GATGATCAACTTGCTCCTAGAAGTCTGATTTAATTTTAAGAAGCTCTGTTATGTTTAAACTGTGTTTATGACATGGAAGAAAGATTTCATCTTATCTGTCAATTCTCATCATTCATTAGTGGTTGTCTGAAGATTGTGTTGAGAAAGATGCTCAAATTAGAAGAAAGTAAACATCTTCCCAGTAGCAATGTTTTCTACAGGCTTTGAACAGATTACTGGTGGCATGTAGCCCTCCTTCCCCATTGCCACTCCTACTCTAAGTTCATCTACCTGAAGTAGTTTTAGGAGGGCAGGTTTCTTGGCCAAAGGAGACCTAAAAA... | GATGATCAACTTGCTCCTAGAAGTCTGATTTAATTTTAAGAAGCTCTGTTATGTTTAAACTGTGTTTATGACATGGAAGAAAGATTTCATCTTATCTGTCAATTCTCATCATTCATTAGTGGTTGTCTGAAGATTGTGTTGAGAAAGATGCTCAAATTAGAAGAAAGTAAACATCTTCCCAGTAGCAATGTTTTCTACAGGCTTTGAACAGATTACTGGTGGCATGTAGCCCTCCTTCCCCATTGCCACTCCTACTCTAAGTTCATCTACCTGAAGTAGTTTTAGGAGGGCAGGTTTCTTGGCCAAAGGAGACCTAAAAA... |
Task1_train_34454 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ATGTAGGGCAAAGATTGGAAAACTTTTTCTCTAAAATGCCAGATAATAAATATTTTTGGCTTTAAGGGCACACAGTCTCCATCCAATTGCCTTTGGAGTAGAAAAGCAGCCACAAGCAATATGTAAACAAACGAGCATGACTGTGTTCCAATAAAACTTTATGAACACTGAAAATTAAAAATTGAAAAATCTGAAGACCATTCTTAGCCTGTGGGCCTGAAAAAAACAGTAGCAGGCTTGATTTAGCCCATGGGCCGTAGTTTACTAACCCCTGCTCCATGGAACTACATTAAATAAGAAAAACATTCAACACTATCACA... | ATGTAGGGCAAAGATTGGAAAACTTTTTCTCTAAAATGCCAGATAATAAATATTTTTGGCTTTAAGGGCACACAGTCTCCATCCAATTGCCTTTGGAGTAGAAAAGCAGCCACAAGCAATATGTAAACAAACGAGCATGACTGTGTTCCAATAAAACTTTATGAACACTGAAAATTAAAAATTGAAAAATCTGAAGACCATTCTTAGCCTGTGGGCCTGAAAAAAACAGTAGCAGGCTTGATTTAGCCCATGGGCCGTAGTTTACTAACCCCTGCTCCATGGAACTACATTAAATAAGAAAAACATTCAACACTATCACA... |
Task1_train_34455 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | AGGGAATGTGGAAAAATGTAGAGACTGATGACATGTCTAAGTTGCCATACAGCCCTGTTCTGCCTAGCCTCAGACCTATTGTATGAAACAATAAACCCCTATTGGTTTAAGCATCTTCAATAATATTTTCTCCTGTTTGCAGCTAAATGGTACCTTAACTGTTCTACTCATTATACCATTGCCATTTTAAAGGATTATACTGGGAATAAGTAGTATTATACTGAGAATAATTCTATTATCTCTGTTTGACTATATAATACATTCATCATATAAAATTACAACTTAAAGTATATGAACTGGACATATATTTGGAAACTCTT... | AGGGAATGTGGAAAAATGTAGAGACTGATGACATGTCTAAGTTGCCATACAGCCCTGTTCTGCCTAGCCTCAGACCTATTGTATGAAACAATAAACCCCTATTGGTTTAAGCATCTTCAATAATATTTTCTCCTGTTTGCAGCTAAATGGTACCTTAACTGTTCTACTCATTATACCATTGCCATTTTAAAGGATTATACTGGGAATAAGTAGTATTATACTGAGAATAATTCTATTATCTCTGTTTGACTATATAATACATTCATCATATAAAATTACAACTTAAAGTATATGAACTGGACATATATTTGGAAACTCTT... |
Task1_train_34456 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGCCCAGATATCCTTCCCTTTACTTTCCTTCTGGTTCAGGCTCCACCCGCTACCACAACCCCAAATCAAAGCCCCATCTTTTAAATATATCTTGCATGGTATTGTTGCTTAGCTAGGGTCCTTACTGCCTAGGATTTGTGAGAAACATAGCAGGCCCTTAGTAATTTGGGAACTACCTATTAAATTCTTCCAGATGACCATTATGTCATCATCAGACATTTCCTTTTCTTACTCTGGCTCAAGGACAAGCCAGAATCTTTTTTTTGGGGGGGGGGGGGTAGTGTCAGCGGGGGACAGATTCTCGCTCTGTCGTTCAGAGT... | AGCCCAGATATCCTTCCCTTTACTTTCCTTCTGGTTCAGGCTCCACCCGCTACCACAACCCCAAATCAAAGCCCCATCTTTTAAATATATCTTGCATGGTATTGTTGCTTAGCTAGGGTCCTTACTGCCTAGGATTTGTGAGAAACATAGCAGGCCCTTAGTAATTTGGGAACTACCTATTAAATTCTTCCAGATGACCATTATGTCATCATCAGACATTTCCTTTTCTTACTCTGGCTCAAGGACAAGCCAGAATCTTTTTTTTGGGGGGGGGGGGGTAGTGTCAGCGGGGGACAGATTCTCGCTCTGTCGTTCAGAGT... |
Task1_train_34457 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | ATAAATACAGTGGTAATTTTATTGTTCTTGAGTTAAATACTGCTGACTTCACCAATACACAGAACTGGTTAGAAAAGCCAAATTAAGATTTTAAAAAATACTGCAAACTAAAAAATGACCCATTTTCATGGTTTCAACATACCAGGCTATGAAATTACTATTTTTAAATGAGCAAAACAGTCAAATAGACAATGTCATATTTGTTGAATCTAATATATCTTCTAATAAAGGAATACTAATTACTATGCTACACTTAGTAGCTTATTTTGTGTTTCTGGAAGTCACATGGACTAAGTGCTAATCATGTTTTATTTTTTGCC... | ATAAATACAGTGGTAATTTTATTGTTCTTGAGTTAAATACTGCTGACTTCACCAATACACAGAACTGGTTAGAAAAGCCAAATTAAGATTTTAAAAAATACTGCAAACTAAAAAATGACCCATTTTCATGGTTTCAACATACCAGGCTATGAAATTACTATTTTTAAATGAGCAAAACAGTCAAATAGACAATGTCATATTTGTTGAATCTAATATATCTTCTAATAAAGGAATACTAATTACTATGCTACACTTAGTAGCTTATTTTGTGTTTCTGGAAGTCACATGGACTAAGTGCTAATCATGTTTTATTTTTTGCC... |
Task1_train_34458 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | TTTAGATTAGTCATGTTGCTTTGAGACTTTTCCATGTTTCCTCTAGACAGCTGCCAATGTTCGCATGGTCTCTGATGAATAAACATGCTGTGACTTGCTTCTAAGGAAACGCCTGTCATGTTCCAGGGAAAAATGACTTCTACACTCTTAAATCAGGAAAACTGTACAAGTCTCATTCATTAGTGACAACGTCGATTTTTCCTTAACGTTTCTATTTCTGGAATGCTCGTATTCTCATTAGGGCATTTCTGCATTCAGATTAACTAAGAAAATAAACTATGTTGGAGGAACACTTATGCTGGGGGGAAAAATCTTGTACT... | TTTAGATTAGTCATGTTGCTTTGAGACTTTTCCATGTTTCCTCTAGACAGCTGCCAATGTTCGCATGGTCTCTGATGAATAAACATGCTGTGACTTGCTTCTAAGGAAACGCCTGTCATGTTCCAGGGAAAAATGACTTCTACACTCTTAAATCAGGAAAACTGTACAAGTCTCATTCATTAGTGACAACGTCGATTTTTCCTTAACGTTTCTATTTCTGGAATGCTCGTATTCTCATTAGGGCATTTCTGCATTCAGATTAACTAAGAAAATAAACTATGTTGGAGGAACACTTATGCTGGGGGGAAAAATCTTGTACT... |
Task1_train_34459 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGCTGCTTCAGACATATGTCTGTGTGTACGCTGTGAAGGTGTTTCTCTTCACAGTTCCCCGCCCTCTAGTGGTAGTTACAATAATGCCATTTTGTAGTCCCTGTACAGGAAATGCCTCTTCTTACTTCAGTTACCAGAATCCTTTTACAGGAAGTTAGGTGTGGTCTTTGAAGGAGAATTAAAAAAAAAAAAAAAAAAAAAAAAAAAAGATTTTTTTTTTTTTAAAGCATGATGGAATTTTAGCTGCAGTCTTCTTGGTGCCAGCTTATCAATCCCAAACTCTGGGTGTAAAAGATTCTACAGGGGTAATGTTTTATTAT... | GGCTGCTTCAGACATATGTCTGTGTGTACGCTGTGAAGGTGTTTCTCTTCACAGTTCCCCGCCCTCTAGTGGTAGTTACAATAATGCCATTTTGTAGTCCCTGTACAGGAAATGCCTCTTCTTACTTCAGTTACCAGAATCCTTTTACAGGAAGTTAGGTGTGGTCTTTGAAGGAGAATTAAAAAAAAAAAAAAAAAAAAAAAAAAAAGATTTTTTTTTTTTTAAAGCATGATGGAATTTTAGCTGCAGTCTTCTTGGTGCCAGCTTATCAATCCCAAACTCTGGGTGTAAAAGATTCTACAGGGGTAATGTTTTATTAT... |
Task1_train_34460 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTTCTTTAGTAGAGTAAGTGGAAATATGAATTGTTTCTCAGACTCTGATTTGACTTGTTAGTGTGGTAAAGAGGGGAGAAGAAAGTCAAGAATGTAATCTCTAAACAAGTTTCAAGATAATCTGGATTTTTTTGAAACCTTTATAAGGTACAATTGACCTTAAATCATTACTTTATTATTTATTTGTGATAAGCTAGGAGTTTAGGAGTTTTGCTTTTTAAAGATTGGTTTGGTATGGGGAATATTTCTTACTGGCCATCTTTTTTGTGTGTTACAGCATTTGATTACTATGCATTTATGTAATGAATGTCAGCAAAAGA... | TTTCTTTAGTAGAGTAAGTGGAAATATGAATTGTTTCTCAGACTCTGATTTGACTTGTTAGTGTGGTAAAGAGGGGAGAAGAAAGTCAAGAATGTAATCTCTAAACAAGTTTCAAGATAATCTGGATTTTTTTGAAACCTTTATAAGGTACAATTGACCTTAAATCATTACTTTATTATTTATTTGTGATAAGCTAGGAGTTTAGGAGTTTTGCTTTTTAAAGATTGGTTTGGTATGGGGAATATTTCTTACTGGCCATCTTTTTTGTGTGTTACAGCATTTGATTACTATGCATTTATGTAATGAATGTCAGCAAAAGA... |
Task1_train_34461 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GAGTAAGTGGAAATATGAATTGTTTCTCAGACTCTGATTTGACTTGTTAGTGTGGTAAAGAGGGGAGAAGAAAGTCAAGAATGTAATCTCTAAACAAGTTTCAAGATAATCTGGATTTTTTTGAAACCTTTATAAGGTACAATTGACCTTAAATCATTACTTTATTATTTATTTGTGATAAGCTAGGAGTTTAGGAGTTTTGCTTTTTAAAGATTGGTTTGGTATGGGGAATATTTCTTACTGGCCATCTTTTTTGTGTGTTACAGCATTTGATTACTATGCATTTATGTAATGAATGTCAGCAAAAGAAGTTGATGCTA... | GAGTAAGTGGAAATATGAATTGTTTCTCAGACTCTGATTTGACTTGTTAGTGTGGTAAAGAGGGGAGAAGAAAGTCAAGAATGTAATCTCTAAACAAGTTTCAAGATAATCTGGATTTTTTTGAAACCTTTATAAGGTACAATTGACCTTAAATCATTACTTTATTATTTATTTGTGATAAGCTAGGAGTTTAGGAGTTTTGCTTTTTAAAGATTGGTTTGGTATGGGGAATATTTCTTACTGGCCATCTTTTTTGTGTGTTACAGCATTTGATTACTATGCATTTATGTAATGAATGTCAGCAAAAGAAGTTGATGCTA... |
Task1_train_34462 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAAGCCAAGAACCAAATGGGAGTTTAGTCATGTGGTGACGGTAGCTAGGGGCAGGAAACAGATAAAGAGTACCTCATGATGTTCTTCTGTCTGCTTTTACATAAATCTGAAATTCTCCATAATAAATGATAGACGATCTTAGCAAAGATGTTACCAAGATGTTCGGCCCTGAGATAGCCATTAATATTTTGTCAGATATGAATAAAAGTTAGACATGCTTGCAAGTCACTTATTCTCAAGATTCTAAGACTATAAACCTTAATCCAAACTGAAGTAAAGGTGACTTTCTATGCAATTTATACTTCATTTGTATCTTGAAA... | AAAGCCAAGAACCAAATGGGAGTTTAGTCATGTGGTGACGGTAGCTAGGGGCAGGAAACAGATAAAGAGTACCTCATGATGTTCTTCTGTCTGCTTTTACATAAATCTGAAATTCTCCATAATAAATGATAGACGATCTTAGCAAAGATGTTACCAAGATGTTCGGCCCTGAGATAGCCATTAATATTTTGTCAGATATGAATAAAAGTTAGACATGCTTGCAAGTCACTTATTCTCAAGATTCTAAGACTATAAACCTTAATCCAAACTGAAGTAAAGGTGACTTTCTATGCAATTTATACTTCATTTGTATCTTGAAA... |
Task1_train_34463 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TAAGCAGCTCTAATGCTAGGGTCAGGGCAGCTGCTTCCAGCTCCAATATTAGCCCCCTACTCCTAAAAGTGGAGGCTGACCTAGATTATTCAGAGACTCATTATAAATACTTGAAGCATCTTTTAAGGGATATAGTCACTAAATCAAAAGAATGTCACATACCTGTGGTATCTTCCATGGACAACTATCAAAATGCAATGGACATGATGATATCTAATAGAATTGTATCTCTAATAAAATGTCTTTAATGTATTCAATCCTTTAAAATATTTAGACTATACAGCCTAAAAGATGGGCACCCTGCTGTTTTTGAGATTTCC... | TAAGCAGCTCTAATGCTAGGGTCAGGGCAGCTGCTTCCAGCTCCAATATTAGCCCCCTACTCCTAAAAGTGGAGGCTGACCTAGATTATTCAGAGACTCATTATAAATACTTGAAGCATCTTTTAAGGGATATAGTCACTAAATCAAAAGAATGTCACATACCTGTGGTATCTTCCATGGACAACTATCAAAATGCAATGGACATGATGATATCTAATAGAATTGTATCTCTAATAAAATGTCTTTAATGTATTCAATCCTTTAAAATATTTAGACTATACAGCCTAAAAGATGGGCACCCTGCTGTTTTTGAGATTTCC... |
Task1_train_34464 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCAGCACAATCACAATTTCTAAAGTGCCCCATGAAAACAAACTGTCACTGGATCTCTTCTTAATTAGAGAGGAAATCCAATGATACCACTTACCTTTTACCTAATACTTACCCTCAATTTTATTGTACATAAGACAATTAGCCAAGAGAAGTCATTTATTTTCTCGATATTTTAAGTGTCTGAGTTAAATGAAAGTCTTAAATGGGTGCACATTTCATTTCATTCCAAAAAACTTAAGGCACTACATGCTTTTTATAGTCATTTCAGCTTTCCCAATTCAAATATCTTGAAAATTAATCCTGTGGAACGCAAAATCATTC... | CCAGCACAATCACAATTTCTAAAGTGCCCCATGAAAACAAACTGTCACTGGATCTCTTCTTAATTAGAGAGGAAATCCAATGATACCACTTACCTTTTACCTAATACTTACCCTCAATTTTATTGTACATAAGACAATTAGCCAAGAGAAGTCATTTATTTTCTCGATATTTTAAGTGTCTGAGTTAAATGAAAGTCTTAAATGGGTGCACATTTCATTTCATTCCAAAAAACTTAAGGCACTACATGCTTTTTATAGTCATTTCAGCTTTCCCAATTCAAATATCTTGAAAATTAATCCTGTGGAACGCAAAATCATTC... |
Task1_train_34465 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | GAATACATTGCATGGTAGACACTATCATGATTTCTACTTGGATGACTCCAGGTAAGGAAAATAGAGCTTTTCTGATCACATTTTCTGTTTCTGAGAGTTGAGACTTGATAGGAAAGGAAAGCCACAGTGGGTCCCTGCAGGTTGTTGGGGAGTGTGCCAAGAATGCCAGGCTCTGCCTGCTCCTTACCTAGGACATTCCTCAGGGTTGTGTTTGCAGTGAGCAACCTTGAGACATGAGGTAGGGTCTCTGGGACAAAGAGCAGGGTTGCTTATGTTGCTTGGTATAAAAGGATGCATTCCCTAAGCTCAGTGTTCCTCAG... | GAATACATTGCATGGTAGACACTATCATGATTTCTACTTGGATGACTCCAGGTAAGGAAAATAGAGCTTTTCTGATCACATTTTCTGTTTCTGAGAGTTGAGACTTGATAGGAAAGGAAAGCCACAGTGGGTCCCTGCAGGTTGTTGGGGAGTGTGCCAAGAATGCCAGGCTCTGCCTGCTCCTTACCTAGGACATTCCTCAGGGTTGTGTTTGCAGTGAGCAACCTTGAGACATGAGGTAGGGTCTCTGGGACAAAGAGCAGGGTTGCTTATGTTGCTTGGTATAAAAGGATGCATTCCCTAAGCTCAGTGTTCCTCAG... |
Task1_train_34466 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTAAAAAGTAACATATATTGTTAAGACTTTGTTAAAAATAACTCTTTACACAGCTTTCGGAAGGTAACTGGCAAACAAGGTTTACAAGTAAAAGATAAACTTTTCAAACTAAAATCAGTTTGTTGTCTTTACGCAATTTACAGAAGCAAGTTATGATTCAATTTAAGTATCTGAAGCAGTTTCCACAATAAAGCATTCCCAAGAAATAGAAAACGGAGCTTAGATAAAGCACCAGCTGTCACATTGTCACCAAGTTAACACTGGTTCCTCACTGGTCTCCATAACATGATGGAGAGCAGGAGAAGAAAGGGAAGGAACAC... | CTAAAAAGTAACATATATTGTTAAGACTTTGTTAAAAATAACTCTTTACACAGCTTTCGGAAGGTAACTGGCAAACAAGGTTTACAAGTAAAAGATAAACTTTTCAAACTAAAATCAGTTTGTTGTCTTTACGCAATTTACAGAAGCAAGTTATGATTCAATTTAAGTATCTGAAGCAGTTTCCACAATAAAGCATTCCCAAGAAATAGAAAACGGAGCTTAGATAAAGCACCAGCTGTCACATTGTCACCAAGTTAACACTGGTTCCTCACTGGTCTCCATAACATGATGGAGAGCAGGAGAAGAAAGGGAAGGAACAC... |
Task1_train_34467 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | ACAATAAAGCATTCCCAAGAAATAGAAAACGGAGCTTAGATAAAGCACCAGCTGTCACATTGTCACCAAGTTAACACTGGTTCCTCACTGGTCTCCATAACATGATGGAGAGCAGGAGAAGAAAGGGAAGGAACACTTAGAGAGGAAAAAAAAAAAACCCTGAAATCTGAAATTACATTTACTTAGGGCATCCCCTAAAGGCATCTTGGTTAGGTTATTCAATTTCTGAGGGGCAGAAAAAGATTATAGTAGTTAAGGCTTGAGATCATGCATTCAGAATAAAATACAATCACTGATACATAAACTATATTGAATGTTAT... | ACAATAAAGCATTCCCAAGAAATAGAAAACGGAGCTTAGATAAAGCACCAGCTGTCACATTGTCACCAAGTTAACACTGGTTCCTCACTGGTCTCCATAACATGATGGAGAGCAGGAGAAGAAAGGGAAGGAACACTTAGAGAGGAAAAAAAAAAAACCCTGAAATCTGAAATTACATTTACTTAGGGCATCCCCTAAAGGCATCTTGGTTAGGTTATTCAATTTCTGAGGGGCAGAAAAAGATTATAGTAGTTAAGGCTTGAGATCATGCATTCAGAATAAAATACAATCACTGATACATAAACTATATTGAATGTTAT... |
Task1_train_34468 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TTTCAAACTAATAGACCAAAGTTTTTGCTATGAGGCTAAAGAATCTGAAAAAAATATTAAAGCACAACACTAAGGTAATTGACAATTACAGTAAAACATTGTTAGGCTTTATTAATCTGGATTTAATTATTTCAGGAATAAAATAATTCCCTGTACTATGATACATAGTGCATTTCCTCTGGAAAGAACTAGAAAGCCAATAAAGTAATTTTATTTCTGTCTACAACTTCAGTACTGTAATTTTATCCATCCTTTTAGTACTTTCTAATTTCTAAATTATGGAAGGTTCTGTCACTTTTGCATTAACACCAGACATTTTT... | TTTCAAACTAATAGACCAAAGTTTTTGCTATGAGGCTAAAGAATCTGAAAAAAATATTAAAGCACAACACTAAGGTAATTGACAATTACAGTAAAACATTGTTAGGCTTTATTAATCTGGATTTAATTATTTCAGGAATAAAATAATTCCCTGTACTATGATACATAGTGCATTTCCTCTGGAAAGAACTAGAAAGCCAATAAAGTAATTTTATTTCTGTCTACAACTTCAGTACTGTAATTTTATCCATCCTTTTAGTACTTTCTAATTTCTAAATTATGGAAGGTTCTGTCACTTTTGCATTAACACCAGACATTTTT... |
Task1_train_34469 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TTTGCTACCCTGAAGAGCTAAAAAAAAAACATTTAAGCCAACTGTGACCGAAACTTTACTTGATTACATGACTATATCTTTATTTTGATTTTGTTGCTTAAGGAAGTAGGTCTTCTGAAATTCCTTTTCTTGTTTTATACATTTTATTATTTTTTCCTGAGCATAAAAGTAGAACATACTTGTAGAAAATTTGGAAAATCCAGAGATAACCAACATTTTTCTTCCTGTATTGTCTTACTATAGTTCTTCCTATATTCCTAAATTACATAATGAAATAATGCCATATGCATGCTTGTACCTTGAATCTTTTTACTTAATGT... | TTTGCTACCCTGAAGAGCTAAAAAAAAAACATTTAAGCCAACTGTGACCGAAACTTTACTTGATTACATGACTATATCTTTATTTTGATTTTGTTGCTTAAGGAAGTAGGTCTTCTGAAATTCCTTTTCTTGTTTTATACATTTTATTATTTTTTCCTGAGCATAAAAGTAGAACATACTTGTAGAAAATTTGGAAAATCCAGAGATAACCAACATTTTTCTTCCTGTATTGTCTTACTATAGTTCTTCCTATATTCCTAAATTACATAATGAAATAATGCCATATGCATGCTTGTACCTTGAATCTTTTTACTTAATGT... |
Task1_train_34470 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAAAAAAACATTTAAGCCAACTGTGACCGAAACTTTACTTGATTACATGACTATATCTTTATTTTGATTTTGTTGCTTAAGGAAGTAGGTCTTCTGAAATTCCTTTTCTTGTTTTATACATTTTATTATTTTTTCCTGAGCATAAAAGTAGAACATACTTGTAGAAAATTTGGAAAATCCAGAGATAACCAACATTTTTCTTCCTGTATTGTCTTACTATAGTTCTTCCTATATTCCTAAATTACATAATGAAATAATGCCATATGCATGCTTGTACCTTGAATCTTTTTACTTAATGTACACTGTGAGAAGTTTCCCAT... | AAAAAAAACATTTAAGCCAACTGTGACCGAAACTTTACTTGATTACATGACTATATCTTTATTTTGATTTTGTTGCTTAAGGAAGTAGGTCTTCTGAAATTCCTTTTCTTGTTTTATACATTTTATTATTTTTTCCTGAGCATAAAAGTAGAACATACTTGTAGAAAATTTGGAAAATCCAGAGATAACCAACATTTTTCTTCCTGTATTGTCTTACTATAGTTCTTCCTATATTCCTAAATTACATAATGAAATAATGCCATATGCATGCTTGTACCTTGAATCTTTTTACTTAATGTACACTGTGAGAAGTTTCCCAT... |
Task1_train_34471 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AATTCATAAGGGAGATGTCAAAACTTGTACTTGGCTCTTTGAAACTCAGCCACTTGATACCATAAAAGATGACTCTGAAACAGCAGTCAAATTGCAAACTGTAAAACAGGAGGAGATCCAAGGTGGGGATGTTCGTACAGCATGTTTTCTTTTTGAGACAGAAAATTTGGACAGCATACAAGGAGAAGAAGTGAAGGAAATCAAGCCTGTTGAAATGGATATACAAGCTGGAGATGTTTCCAGCATGAGGTATAAATTTGAAAATCAGTCCTTAGATTCTATAAGTTCTAGTTCAGAGGAAGTTTTGAAAAAGATCAAAA... | AATTCATAAGGGAGATGTCAAAACTTGTACTTGGCTCTTTGAAACTCAGCCACTTGATACCATAAAAGATGACTCTGAAACAGCAGTCAAATTGCAAACTGTAAAACAGGAGGAGATCCAAGGTGGGGATGTTCGTACAGCATGTTTTCTTTTTGAGACAGAAAATTTGGACAGCATACAAGGAGAAGAAGTGAAGGAAATCAAGCCTGTTGAAATGGATATACAAGCTGGAGATGTTTCCAGCATGAGGTATAAATTTGAAAATCAGTCCTTAGATTCTATAAGTTCTAGTTCAGAGGAAGTTTTGAAAAAGATCAAAA... |
Task1_train_34472 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGACCGAGAAGGGTCCTATCATGAAGTGACCACAGTTAAAAAAGAAGAGGTAATTCATGGAGATGTGCGAGGAACAAGGTGGCTTTTTGAAACAAAGCCATTAGACTCTATTAATAAATCAGAAACTGTGTATGTTATTAAATCTGTCACACAAGAAGACATTCAGAAGGGAGATGTTAGTTCTGTCAGATACAGATTTGAAACTCAGCCACTGGATCAGATTTCTGAAGAATCACATAATATTATGCCCAGTATTGACCATATACAAGGTGGCAATGTAAAGACAAGTAGACAATTCTTTGAGTCTGAAAATTTTGATA... | AGACCGAGAAGGGTCCTATCATGAAGTGACCACAGTTAAAAAAGAAGAGGTAATTCATGGAGATGTGCGAGGAACAAGGTGGCTTTTTGAAACAAAGCCATTAGACTCTATTAATAAATCAGAAACTGTGTATGTTATTAAATCTGTCACACAAGAAGACATTCAGAAGGGAGATGTTAGTTCTGTCAGATACAGATTTGAAACTCAGCCACTGGATCAGATTTCTGAAGAATCACATAATATTATGCCCAGTATTGACCATATACAAGGTGGCAATGTAAAGACAAGTAGACAATTCTTTGAGTCTGAAAATTTTGATA... |
Task1_train_34473 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTACTCTCAAAAAGTTATCCAGGCTCCTGGAATCATCATTGAAGCTGATGAAATAGGGGATGTTCGAATGGCAAAATACAAGCTAATGAACCAAGCATCTCCTGAGATACAGAAAGAAGAAATTATCAGGGCTGATCTCAGAAATATAATGGTGAACCTACTTTCCAAAAGGGACTGTACTGAAAGAGAGATTTTGATTAGTGAAGAAGAGAAGGGAAATGTTAATTTGACTAAAACTCAATTATTAAACAGATCAACTGAATTTCATGCTGAAAAAGAAGAGATAGTGAAAGGTGATGTACAACAAGCAATAAAAAACC... | CTACTCTCAAAAAGTTATCCAGGCTCCTGGAATCATCATTGAAGCTGATGAAATAGGGGATGTTCGAATGGCAAAATACAAGCTAATGAACCAAGCATCTCCTGAGATACAGAAAGAAGAAATTATCAGGGCTGATCTCAGAAATATAATGGTGAACCTACTTTCCAAAAGGGACTGTACTGAAAGAGAGATTTTGATTAGTGAAGAAGAGAAGGGAAATGTTAATTTGACTAAAACTCAATTATTAAACAGATCAACTGAATTTCATGCTGAAAAAGAAGAGATAGTGAAAGGTGATGTACAACAAGCAATAAAAAACC... |
Task1_train_34474 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ACAGGGCAGTGAGAGAGCTGAAGAAGGATGATGTCTTTAATTCCATCCAATCTGCTGGTAAAACCGTTGGAAAGCAACAGACATATGAACTGAGAAATGACCACCAGAAAATGGAGGGTTTTCATATAAAGAGTCCTAAAAAGACCAAAAATATTAAAATATTAACTGATACACAAAGCTCCAAGCCCAGTCCCACCCAGCATCCAGTCAGCATGCCAGTTGGAGGAACTTACGACCTTTCAGGGGACTTTCAGAAGCAAACTTTGTTAAAGCAAGAAACAAAATATTCTAATAAGGATATAAAGAAAAAGAATATAAAC... | ACAGGGCAGTGAGAGAGCTGAAGAAGGATGATGTCTTTAATTCCATCCAATCTGCTGGTAAAACCGTTGGAAAGCAACAGACATATGAACTGAGAAATGACCACCAGAAAATGGAGGGTTTTCATATAAAGAGTCCTAAAAAGACCAAAAATATTAAAATATTAACTGATACACAAAGCTCCAAGCCCAGTCCCACCCAGCATCCAGTCAGCATGCCAGTTGGAGGAACTTACGACCTTTCAGGGGACTTTCAGAAGCAAACTTTGTTAAAGCAAGAAACAAAATATTCTAATAAGGATATAAAGAAAAAGAATATAAAC... |
Task1_train_34475 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CGAACTCTCAGAATTCTCAGGCTAAAATCATAACAGGAAAAACCGGTGTGTTGCCACCTCCCACATTGCCCAAACCCAAACTTCCCAAGCATATAAAAGATAATAAGAACGATTTTTCCCCCAAAGTTGAACTGGCAACCTCCCTGTCAGATATGGAATGTAAAATTACTACCTCAAAGGATCAGAAAAAAGTAATGGTGATGACCAGCAGTGAACACACGGAGACAAAGCAGAACGTTATTAGTAAGAGTCTTGATGAAAGAAAACAATTATCTATTGACTCTGCAAACTGTCTCTCACACACAGTTCCAGGAACTTCA... | CGAACTCTCAGAATTCTCAGGCTAAAATCATAACAGGAAAAACCGGTGTGTTGCCACCTCCCACATTGCCCAAACCCAAACTTCCCAAGCATATAAAAGATAATAAGAACGATTTTTCCCCCAAAGTTGAACTGGCAACCTCCCTGTCAGATATGGAATGTAAAATTACTACCTCAAAGGATCAGAAAAAAGTAATGGTGATGACCAGCAGTGAACACACGGAGACAAAGCAGAACGTTATTAGTAAGAGTCTTGATGAAAGAAAACAATTATCTATTGACTCTGCAAACTGTCTCTCACACACAGTTCCAGGAACTTCA... |
Task1_train_34476 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCTCTTTTAGTTTTCATATGCTGATCAAGAAAATAAGGCAGCTTGATTTCCAGAATTCCCTGGCTTGGCTCCTCTTCTCCATATTTTTCAGAACCTTCTCTTTCATTTCTGTAATCATTATCCTGCTCAATCTTGATTCTACTCTCCTATTTTTTCTCACTTTGGGATTCTGTTTAAAAGGGGAGCCCAGTTTTAGGAGTTCAACCTCACTAGCCTCTTCAAGTCTTCCTTACCACAGGGACCTTGCACTCATTGTCTATTGGAGATCACAAATCTCCTCAAAGTTTCAGCTGCTGTTCTCTGATTGGCATGTGATACTT... | CCTCTTTTAGTTTTCATATGCTGATCAAGAAAATAAGGCAGCTTGATTTCCAGAATTCCCTGGCTTGGCTCCTCTTCTCCATATTTTTCAGAACCTTCTCTTTCATTTCTGTAATCATTATCCTGCTCAATCTTGATTCTACTCTCCTATTTTTTCTCACTTTGGGATTCTGTTTAAAAGGGGAGCCCAGTTTTAGGAGTTCAACCTCACTAGCCTCTTCAAGTCTTCCTTACCACAGGGACCTTGCACTCATTGTCTATTGGAGATCACAAATCTCCTCAAAGTTTCAGCTGCTGTTCTCTGATTGGCATGTGATACTT... |
Task1_train_34477 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GTTTCTCCTTAGTTCTTTGTATTTTGATGTTGAGGGGGCTATCTTGTCACTTCATTTAGTTGTAAATGTTCCCCATGGGTTTTAAGTTTTGCTATCTTGTTGATGTATCTGTTTTTATGTGTAGATTCATAGATATTTCGAAAACTATGCTCCTGCCTCTGACTAGAGTTCATTTTAATTTTAAATCACTCAATTTGTTAATCTCCTTAAAGAGGCCACATAAGCAATTGTTAGGCACACCTTCCAGCTCGTTCAAAATCCAGTTAACAAAGAAGCTCATATTGTTGATTTGTATGTGTTTGCTACTCAGGATTTATTGG... | GTTTCTCCTTAGTTCTTTGTATTTTGATGTTGAGGGGGCTATCTTGTCACTTCATTTAGTTGTAAATGTTCCCCATGGGTTTTAAGTTTTGCTATCTTGTTGATGTATCTGTTTTTATGTGTAGATTCATAGATATTTCGAAAACTATGCTCCTGCCTCTGACTAGAGTTCATTTTAATTTTAAATCACTCAATTTGTTAATCTCCTTAAAGAGGCCACATAAGCAATTGTTAGGCACACCTTCCAGCTCGTTCAAAATCCAGTTAACAAAGAAGCTCATATTGTTGATTTGTATGTGTTTGCTACTCAGGATTTATTGG... |
Task1_train_34478 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | GTTGAGGGGGCTATCTTGTCACTTCATTTAGTTGTAAATGTTCCCCATGGGTTTTAAGTTTTGCTATCTTGTTGATGTATCTGTTTTTATGTGTAGATTCATAGATATTTCGAAAACTATGCTCCTGCCTCTGACTAGAGTTCATTTTAATTTTAAATCACTCAATTTGTTAATCTCCTTAAAGAGGCCACATAAGCAATTGTTAGGCACACCTTCCAGCTCGTTCAAAATCCAGTTAACAAAGAAGCTCATATTGTTGATTTGTATGTGTTTGCTACTCAGGATTTATTGGAAATTACAACGCCTCACATAAATCATTG... | GTTGAGGGGGCTATCTTGTCACTTCATTTAGTTGTAAATGTTCCCCATGGGTTTTAAGTTTTGCTATCTTGTTGATGTATCTGTTTTTATGTGTAGATTCATAGATATTTCGAAAACTATGCTCCTGCCTCTGACTAGAGTTCATTTTAATTTTAAATCACTCAATTTGTTAATCTCCTTAAAGAGGCCACATAAGCAATTGTTAGGCACACCTTCCAGCTCGTTCAAAATCCAGTTAACAAAGAAGCTCATATTGTTGATTTGTATGTGTTTGCTACTCAGGATTTATTGGAAATTACAACGCCTCACATAAATCATTG... |
Task1_train_34479 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAAACAATAAGGAAAATATGTTATCCTTCGGACCCAAACATTCTGTAAATATCATTCTGAAAAGAGATTACATGCATTTATTCATTTCTCAGGAATGATTCTACATTCCTTGAAACTGTAACACTTCCGTAATCAAGTAAAAAATTTTTCTATTTATCAGCTTTACCTGCTATTTGTACTGAACCATCCTCACCCAGAAGAATATTACCAGCTTTCAAATCCCTATTAGAAAAAAAAATAGAAAATAAATTGTAGGGTACAGACTTTATAGTGTATTGATTCACTCAGGAAGATTTTAAAACATATCATACAACGCAGCT... | AAAACAATAAGGAAAATATGTTATCCTTCGGACCCAAACATTCTGTAAATATCATTCTGAAAAGAGATTACATGCATTTATTCATTTCTCAGGAATGATTCTACATTCCTTGAAACTGTAACACTTCCGTAATCAAGTAAAAAATTTTTCTATTTATCAGCTTTACCTGCTATTTGTACTGAACCATCCTCACCCAGAAGAATATTACCAGCTTTCAAATCCCTATTAGAAAAAAAAATAGAAAATAAATTGTAGGGTACAGACTTTATAGTGTATTGATTCACTCAGGAAGATTTTAAAACATATCATACAACGCAGCT... |
Task1_train_34480 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GAGGCCCTGTGCCTGTCTTTAACGCGCCTTTCACTCTGTAGCCATGACCCTGTTTAAGACGCTTCAAAGACTCCTATGACCTTTAGGATAAAATTTAGCCCTCATCATTTTATAAAAGGGCCTTCGAGAGCTGAACTCTGCCTTCCTGTTTACTTTCTCTCTTTCCGTCTCCCCATGATCCCTGCCTCTCTCCTTACTGGGCCACTTGCAATCCCACCCCATTTGCACCCCACTCACACTCCTGCATCACCACCACCACCACCACACGTGGGTCCCTGCATTTGCACAGGCTGTATTGCCTGCCTGGTAGATGTTTCATC... | GAGGCCCTGTGCCTGTCTTTAACGCGCCTTTCACTCTGTAGCCATGACCCTGTTTAAGACGCTTCAAAGACTCCTATGACCTTTAGGATAAAATTTAGCCCTCATCATTTTATAAAAGGGCCTTCGAGAGCTGAACTCTGCCTTCCTGTTTACTTTCTCTCTTTCCGTCTCCCCATGATCCCTGCCTCTCTCCTTACTGGGCCACTTGCAATCCCACCCCATTTGCACCCCACTCACACTCCTGCATCACCACCACCACCACCACACGTGGGTCCCTGCATTTGCACAGGCTGTATTGCCTGCCTGGTAGATGTTTCATC... |
Task1_train_34481 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | TTTGCATAATAATGTGAATGCACTTAATGACACTGAAATGGATGCCTAAGGTGGATAAAATGGCATGTCATATTATGTAAATTTTACCATAATTAAAAGTATAAAGAAATTTAAAATAATTTTAATCACCATATACCATAGATGAATTAACAACACAGGGATATAGAGGAATACCATACTGAATCAGGCCAATGGGCTCCTGTAGGAATTTCAAGAGGTGAGCAAGGAGAACCCAGTGATCTTTGTGACTCTCCATTCTCACCTCTCTTGCACTGCCAAGGGCCTTGAGACATACCCATCTTTCTTCTTCCCTATGGTCG... | TTTGCATAATAATGTGAATGCACTTAATGACACTGAAATGGATGCCTAAGGTGGATAAAATGGCATGTCATATTATGTAAATTTTACCATAATTAAAAGTATAAAGAAATTTAAAATAATTTTAATCACCATATACCATAGATGAATTAACAACACAGGGATATAGAGGAATACCATACTGAATCAGGCCAATGGGCTCCTGTAGGAATTTCAAGAGGTGAGCAAGGAGAACCCAGTGATCTTTGTGACTCTCCATTCTCACCTCTCTTGCACTGCCAAGGGCCTTGAGACATACCCATCTTTCTTCTTCCCTATGGTCG... |
Task1_train_34482 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTCAGCACACACACACGTGTCACTGTACCTGCATGTTCAAGTATAATTACCATAATCTTGACTATCTAGTTTTTTAAATTAGAAATTGGTTTAAAAAAAAAAAAAAGAACTTCAGTAAAACCAGGACATTATGGTTCACACAATATATTAAGGAGTCACTGTTGCATTGTTTGAGAAACAGTTCCATACACAGCTAGGGATGATGATAACATGCACATGCCCCAAATATCCCGTATTTATACCTGAATGGCAAAACTGGTGAATGTTTTCCAAAACATGCATGCAATTACTATTATTATACAATGATGTTTTTCTCTAGA... | TTCAGCACACACACACGTGTCACTGTACCTGCATGTTCAAGTATAATTACCATAATCTTGACTATCTAGTTTTTTAAATTAGAAATTGGTTTAAAAAAAAAAAAAAGAACTTCAGTAAAACCAGGACATTATGGTTCACACAATATATTAAGGAGTCACTGTTGCATTGTTTGAGAAACAGTTCCATACACAGCTAGGGATGATGATAACATGCACATGCCCCAAATATCCCGTATTTATACCTGAATGGCAAAACTGGTGAATGTTTTCCAAAACATGCATGCAATTACTATTATTATACAATGATGTTTTTCTCTAGA... |
Task1_train_34483 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | AGGTCAGTTTCACCTTTTCTCTATACTGTATTCCTGCCTCCAATGACCAAACCTGAAAAAATATGTTTCTTCTAAGAAAAAAATTCTCATAACTCCTTTTTAGTTTTTATAACTGCAGTATTTTCTTCATCTATAAAATTTTACTGAGTGTGTGCTTCTTACCTTTACATTACCAAATTCTTGTTTATTCTTCTTCCACATTGGTATCCCACTTACTTCTTCTTTCAAAGCCTCATTTCTCTGTGTTCCTTAGCATTTATATAACCAAATTTCAGTCTGATTATCAGGAACAAACCATTCAAGGATTCCTAGAACTCAAT... | AGGTCAGTTTCACCTTTTCTCTATACTGTATTCCTGCCTCCAATGACCAAACCTGAAAAAATATGTTTCTTCTAAGAAAAAAATTCTCATAACTCCTTTTTAGTTTTTATAACTGCAGTATTTTCTTCATCTATAAAATTTTACTGAGTGTGTGCTTCTTACCTTTACATTACCAAATTCTTGTTTATTCTTCTTCCACATTGGTATCCCACTTACTTCTTCTTTCAAAGCCTCATTTCTCTGTGTTCCTTAGCATTTATATAACCAAATTTCAGTCTGATTATCAGGAACAAACCATTCAAGGATTCCTAGAACTCAAT... |
Task1_train_34484 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTTTTTTATGTTTTTTGTGCATTGCTGTTTTTAATCCAAAGTGTATAACCTATAGGTCAATTCCCCTGTTCTCTATTTTCTGTGTCTCAAAAAAAAAAAAACAAACAAAACAAAACCCAAAACAAAAGAAAAAAAAAAAACAAGAAACAAGGACTTTTGAAAATCTGTGCAATTAAACCCAATGAAAAAATTTGCCCCAGATGGAATGCTCATGCGCTTTTCATCTGGATGGTAGCTGCGTTTCTACTGAGTTTTCCTCAAGCAAAGAAAGGTTGAGAGAGGAGGCACATAGGGCAGGGCGTGAAAATATATATGGTTCA... | TTTTTTTATGTTTTTTGTGCATTGCTGTTTTTAATCCAAAGTGTATAACCTATAGGTCAATTCCCCTGTTCTCTATTTTCTGTGTCTCAAAAAAAAAAAAACAAACAAAACAAAACCCAAAACAAAAGAAAAAAAAAAAACAAGAAACAAGGACTTTTGAAAATCTGTGCAATTAAACCCAATGAAAAAATTTGCCCCAGATGGAATGCTCATGCGCTTTTCATCTGGATGGTAGCTGCGTTTCTACTGAGTTTTCCTCAAGCAAAGAAAGGTTGAGAGAGGAGGCACATAGGGCAGGGCGTGAAAATATATATGGTTCA... |
Task1_train_34485 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | GCTGTCATGAGGCCATGGGCAGTGCATGTGCTAGGCAGGTTTACCTCTCTCATCCACTAGAAACACCATCCCTTTTCAGAAACTGACAACATCTGTCTCTCCCCTTCTCTGAAGCTGTGTACCACTTCTCACTGCAAATAAAAACAACTAACTTGGGGGACTAAATACTATCTTTCTCAACATTATTATTTAGGAAATTTGTGGCTGTTATGTATTAAATTGTTCTTGAATTTAAAATATATTGCTGAAAAGGAACTTAGCCATCAGAAAAACTGAAACCAAAGAAACAAGATACATATTAACACTTCATTTAGTCATCT... | GCTGTCATGAGGCCATGGGCAGTGCATGTGCTAGGCAGGTTTACCTCTCTCATCCACTAGAAACACCATCCCTTTTCAGAAACTGACAACATCTGTCTCTCCCCTTCTCTGAAGCTGTGTACCACTTCTCACTGCAAATAAAAACAACTAACTTGGGGGACTAAATACTATCTTTCTCAACATTATTATTTAGGAAATTTGTGGCTGTTATGTATTAAATTGTTCTTGAATTTAAAATATATTGCTGAAAAGGAACTTAGCCATCAGAAAAACTGAAACCAAAGAAACAAGATACATATTAACACTTCATTTAGTCATCT... |
Task1_train_34486 | This genomic variant is located on Chromosome 2. Can you determine its pathogenicity and name any linked disease? | Benign | GAAATGTGTATAATTGTGCAACTTTTTTTCCTTCTATGACCTCTTAGTTTCTCCCAGGAATGTATGGCTAGGGGTACCTGTGGCAGGTCCATGATGAAGTTGTAGGCATTGGCCTCCTTGGCAGCTTGGACTATGTCTTCCATTGTTGCATCTTCTCTGCCATAGCGAATATTTTCTGCAATGGTGGTAGAGAACAGAACTGGCTCTTGCTCCACTATCCCAATCTGATCTCTAAGCCACTGAATGTTAAGAGAGCGAATGTCATGGCCATCCACGGTCACCTAGAGAGCATGGGCACAACATCACAACTTTTGGAATCT... | GAAATGTGTATAATTGTGCAACTTTTTTTCCTTCTATGACCTCTTAGTTTCTCCCAGGAATGTATGGCTAGGGGTACCTGTGGCAGGTCCATGATGAAGTTGTAGGCATTGGCCTCCTTGGCAGCTTGGACTATGTCTTCCATTGTTGCATCTTCTCTGCCATAGCGAATATTTTCTGCAATGGTGGTAGAGAACAGAACTGGCTCTTGCTCCACTATCCCAATCTGATCTCTAAGCCACTGAATGTTAAGAGAGCGAATGTCATGGCCATCCACGGTCACCTAGAGAGCATGGGCACAACATCACAACTTTTGGAATCT... |
Task1_train_34487 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | GCAGTGCTGCCATACTGAAAGTTAATTTTGGAATCCAGAACTCTGTTGGCAAGAATGCTATTCACTTATAGTAAATATAATATTCACTATTATATCCTAGATATAATATCTATATCCAGATATTGACCTGGGTGCTTTCCCAATTTTTTTCATGGCCCACAAAGAATACAGGATATGATAATGTCTCCATGACATGCTGGGGTAAGTGGAGGTAGTTGCTGGGGCTTCAGCAAGCCCAACCACTGCCCAGCTGCACCCATGGCTGAGTGTACTCATATCCAGGCCCAGACTCACTCATGGCCCATGGAGTGCAGTAGAGA... | GCAGTGCTGCCATACTGAAAGTTAATTTTGGAATCCAGAACTCTGTTGGCAAGAATGCTATTCACTTATAGTAAATATAATATTCACTATTATATCCTAGATATAATATCTATATCCAGATATTGACCTGGGTGCTTTCCCAATTTTTTTCATGGCCCACAAAGAATACAGGATATGATAATGTCTCCATGACATGCTGGGGTAAGTGGAGGTAGTTGCTGGGGCTTCAGCAAGCCCAACCACTGCCCAGCTGCACCCATGGCTGAGTGTACTCATATCCAGGCCCAGACTCACTCATGGCCCATGGAGTGCAGTAGAGA... |
Task1_train_34488 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GATCCGCCTGCCTTGGCCTCCCAAAGCGCTAGGATTACAGGCGTGAGCCACCGCGCCTGGCCTGATCCAGATTTTTTGAAGAGACATATCTCCTTTGATACAGCAGCACCATTTCTGGACATCTAGACCATAAGGATCTTTCCACATGTGCACAAAGGATGTTCACCCTGACACTGTTTTTCATAGTGAAAAAATGGAAACAACCTAAATGTCCAACCACTAGGAAAAGGATAAAAATACATGGACCATTCGCATTTTAAAATATTCTTTGGCAGTGTACAGGAATGAGGCTGGTCTGTATTTGCTGACATGATGTTAAG... | GATCCGCCTGCCTTGGCCTCCCAAAGCGCTAGGATTACAGGCGTGAGCCACCGCGCCTGGCCTGATCCAGATTTTTTGAAGAGACATATCTCCTTTGATACAGCAGCACCATTTCTGGACATCTAGACCATAAGGATCTTTCCACATGTGCACAAAGGATGTTCACCCTGACACTGTTTTTCATAGTGAAAAAATGGAAACAACCTAAATGTCCAACCACTAGGAAAAGGATAAAAATACATGGACCATTCGCATTTTAAAATATTCTTTGGCAGTGTACAGGAATGAGGCTGGTCTGTATTTGCTGACATGATGTTAAG... |
Task1_train_34489 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGAAAAGCTGCTCAGGGCAGGGCTCTGAGCAACACCAATACTCAAGGGCTGAGTAGAAGAGGAAAATAAAATGGAATGACCAAAGCAGCTCAAAAGAGAGCCAGGACTGCTGGGAGTCATGGCAGCCAAGGGAGTGGTGTCAAGAAGGAGGAATGGTCTCCAGAGTCAAGTGCAATCTAAATGCCCATCCAGTGTGAGAAGGAAGGAAAAGTGCCCATTGGCAATCAGGAGTTATCTGGTAACTTTAGTGAATACAGAGGTGGCATATTTTGTTTGTGGTTAAAAGATATCTAATGGAGAATTTTTATATCATTAAAAAT... | AGAAAAGCTGCTCAGGGCAGGGCTCTGAGCAACACCAATACTCAAGGGCTGAGTAGAAGAGGAAAATAAAATGGAATGACCAAAGCAGCTCAAAAGAGAGCCAGGACTGCTGGGAGTCATGGCAGCCAAGGGAGTGGTGTCAAGAAGGAGGAATGGTCTCCAGAGTCAAGTGCAATCTAAATGCCCATCCAGTGTGAGAAGGAAGGAAAAGTGCCCATTGGCAATCAGGAGTTATCTGGTAACTTTAGTGAATACAGAGGTGGCATATTTTGTTTGTGGTTAAAAGATATCTAATGGAGAATTTTTATATCATTAAAAAT... |
Task1_train_34490 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGGTGACAGAGCGAGACTCTGTCTCAAAAATAAATAAATAAATGAAAGTATTTAATGAAGTATATTATACCATCTATATATAAACAAAGGACCGATTTTCTTTCAAATCATTACTTCTACCTCCATAATTAATATGGTATTCTATTATAATCAACAGCCTACGTTATGTCCCCAGTTATATACTCTTTAAAAAAAGGGGGGGCTGTTCTCTATGACCATTGTAGGAGTTCATCTTGATTTTGCTGTGTTTAGTGATAACATTGTTCTCATGGGGTTATATCTGTTCTATTTTTCACGTTTTATTTAATGAATGATAATTT... | GGGTGACAGAGCGAGACTCTGTCTCAAAAATAAATAAATAAATGAAAGTATTTAATGAAGTATATTATACCATCTATATATAAACAAAGGACCGATTTTCTTTCAAATCATTACTTCTACCTCCATAATTAATATGGTATTCTATTATAATCAACAGCCTACGTTATGTCCCCAGTTATATACTCTTTAAAAAAAGGGGGGGCTGTTCTCTATGACCATTGTAGGAGTTCATCTTGATTTTGCTGTGTTTAGTGATAACATTGTTCTCATGGGGTTATATCTGTTCTATTTTTCACGTTTTATTTAATGAATGATAATTT... |
Task1_train_34491 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GAGGCAGGAGAATCACTTGAACCCAGGAGACAGAGGTTGCAATGAGCCAAGATCGCACCACTACACTCCAGCCTGGGCGACAGAGCAAGACTCTGTCTCAAAAACAAACAAACAAACAAAAAACCTTTTTTTAGGTAGATAATTCATGTCTATTATGGTTACCCTTTAAATGAGGGACATCTCCTAGCTCAGCAGCAACAAGTATCCTCTGACTTATTCACTCAATGTATTACCAAACAATATACCTACCTAAGTAAGAATTAAGATGTTGCACGCAAGTTCCCAAAAATTCATCCCTTTGAGGTGGATCATAGTTCAAT... | GAGGCAGGAGAATCACTTGAACCCAGGAGACAGAGGTTGCAATGAGCCAAGATCGCACCACTACACTCCAGCCTGGGCGACAGAGCAAGACTCTGTCTCAAAAACAAACAAACAAACAAAAAACCTTTTTTTAGGTAGATAATTCATGTCTATTATGGTTACCCTTTAAATGAGGGACATCTCCTAGCTCAGCAGCAACAAGTATCCTCTGACTTATTCACTCAATGTATTACCAAACAATATACCTACCTAAGTAAGAATTAAGATGTTGCACGCAAGTTCCCAAAAATTCATCCCTTTGAGGTGGATCATAGTTCAAT... |
Task1_train_34492 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | TCATCAATGTTATGTAGTACTACTTTCCCTTGCAGTTTTTAGATTTGGCCATGTTTGGTCTGTCTTCTCATCATTTCTAAAGCATGCTATGTTTCTTCTTAACTCAGAACCTTCCTGTCAGCATCTTTTCCCTTTTCCTTTTATACCCATTCTATTATAGCTGCATATATGTTTAACATATGTGATTATATGTTCATTCACATGCTCTCCAAGTCCTGTAGAATATGAGTTCCAGGAAAGCACACTCATATATCTTGGCTCACTGATGTTCTCTCAGTATGTAATAAGAGTGTTTGGTCATCCTAAGGGTTGAATAAGTG... | TCATCAATGTTATGTAGTACTACTTTCCCTTGCAGTTTTTAGATTTGGCCATGTTTGGTCTGTCTTCTCATCATTTCTAAAGCATGCTATGTTTCTTCTTAACTCAGAACCTTCCTGTCAGCATCTTTTCCCTTTTCCTTTTATACCCATTCTATTATAGCTGCATATATGTTTAACATATGTGATTATATGTTCATTCACATGCTCTCCAAGTCCTGTAGAATATGAGTTCCAGGAAAGCACACTCATATATCTTGGCTCACTGATGTTCTCTCAGTATGTAATAAGAGTGTTTGGTCATCCTAAGGGTTGAATAAGTG... |
Task1_train_34493 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGGTACACCCTTGCAAGAGAATACTATGTCAGTTGGAAAAGAAGATATTTATATCTGCTGTGTTGTGTCTCTAAGCTATATTAAGTGAAAAGAACGAAGTTATTTTGTGTAAGTAAAATATATGTGTATTTGCTTTTAAAGAGAAATAAGCAAAGGATACAACAGTGAAATGGCAACCTAAGGAAGGAAAAGTATTTGCAAATCATTTATCTGAAAAGGGATCAATCTAGAATACATAATAACTACAACTCAACAACAAAACAAATAACATGAAAAAAATGGGCAAAGGACTTGGAACAGATATTTCTCCAAAGATGATA... | GGGTACACCCTTGCAAGAGAATACTATGTCAGTTGGAAAAGAAGATATTTATATCTGCTGTGTTGTGTCTCTAAGCTATATTAAGTGAAAAGAACGAAGTTATTTTGTGTAAGTAAAATATATGTGTATTTGCTTTTAAAGAGAAATAAGCAAAGGATACAACAGTGAAATGGCAACCTAAGGAAGGAAAAGTATTTGCAAATCATTTATCTGAAAAGGGATCAATCTAGAATACATAATAACTACAACTCAACAACAAAACAAATAACATGAAAAAAATGGGCAAAGGACTTGGAACAGATATTTCTCCAAAGATGATA... |
Task1_train_34494 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | GGATGAATATTATGTGAGGAAACAAGAAATTTCTCTCCCCATGTTTGGGAAATACTTCAATACTGATATGCCTATTTGGTGATGAGAAACAGACATAATGTGACTTATTAAGAAATCAGTAAGCAGGCTTAGCTTCAGATCCAGCAGTTCCTGGACTCCCATCCTACCCGTTCCCTCTGAGGTTCCTGGGGGTGTGCACAACTACCGGGTGCATCTTCAGTAGGAACTCTCAGAGGACATAGGGGCTATGTTTATCTTAGGAGTTTTTATACACTATTCCTAATGCTAGGAGGACTGGGCCATACACCTATGTTACTGAC... | GGATGAATATTATGTGAGGAAACAAGAAATTTCTCTCCCCATGTTTGGGAAATACTTCAATACTGATATGCCTATTTGGTGATGAGAAACAGACATAATGTGACTTATTAAGAAATCAGTAAGCAGGCTTAGCTTCAGATCCAGCAGTTCCTGGACTCCCATCCTACCCGTTCCCTCTGAGGTTCCTGGGGGTGTGCACAACTACCGGGTGCATCTTCAGTAGGAACTCTCAGAGGACATAGGGGCTATGTTTATCTTAGGAGTTTTTATACACTATTCCTAATGCTAGGAGGACTGGGCCATACACCTATGTTACTGAC... |
Task1_train_34495 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTGTGTTCCAATAATGGAACACCAAGCATAAATGGGTTTTAATCAGCTGCATGTTCTAAGTCAGTTTTCTCACCTGTAAAATGAGGATAATAATATCCTCTTCATAGTTTTGTTTTTAGAATCAAAGAGACATTTTATGAAAAAATTTAAAGCACACTATCTTACATTACTATTCCTACTTCTTCAACTACTTTTCCTTGCTCTTTCCTAGGCGTAGTGGTTTCCTATATTGTGGAGGAATTCACCACATCAAATTCTGAAGAGTACTCTTCCAGTTATCCTTGTGGGTAGATAGGTGGGAGAATAAATAAGCAACAGCT... | TTGTGTTCCAATAATGGAACACCAAGCATAAATGGGTTTTAATCAGCTGCATGTTCTAAGTCAGTTTTCTCACCTGTAAAATGAGGATAATAATATCCTCTTCATAGTTTTGTTTTTAGAATCAAAGAGACATTTTATGAAAAAATTTAAAGCACACTATCTTACATTACTATTCCTACTTCTTCAACTACTTTTCCTTGCTCTTTCCTAGGCGTAGTGGTTTCCTATATTGTGGAGGAATTCACCACATCAAATTCTGAAGAGTACTCTTCCAGTTATCCTTGTGGGTAGATAGGTGGGAGAATAAATAAGCAACAGCT... |
Task1_train_34496 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ATAATGGAACACCAAGCATAAATGGGTTTTAATCAGCTGCATGTTCTAAGTCAGTTTTCTCACCTGTAAAATGAGGATAATAATATCCTCTTCATAGTTTTGTTTTTAGAATCAAAGAGACATTTTATGAAAAAATTTAAAGCACACTATCTTACATTACTATTCCTACTTCTTCAACTACTTTTCCTTGCTCTTTCCTAGGCGTAGTGGTTTCCTATATTGTGGAGGAATTCACCACATCAAATTCTGAAGAGTACTCTTCCAGTTATCCTTGTGGGTAGATAGGTGGGAGAATAAATAAGCAACAGCTGCAACCCCTT... | ATAATGGAACACCAAGCATAAATGGGTTTTAATCAGCTGCATGTTCTAAGTCAGTTTTCTCACCTGTAAAATGAGGATAATAATATCCTCTTCATAGTTTTGTTTTTAGAATCAAAGAGACATTTTATGAAAAAATTTAAAGCACACTATCTTACATTACTATTCCTACTTCTTCAACTACTTTTCCTTGCTCTTTCCTAGGCGTAGTGGTTTCCTATATTGTGGAGGAATTCACCACATCAAATTCTGAAGAGTACTCTTCCAGTTATCCTTGTGGGTAGATAGGTGGGAGAATAAATAAGCAACAGCTGCAACCCCTT... |
Task1_train_34497 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | ACGCATTTCTCTTGTTTATCTGTCTCTTGTTCTAGGGGCCTCAGCTGTGAACTTGGATGGGTGAGGAAAAGATATTTTTCCTGGCTGGGCAAGGTGGCTCACGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCATGAGGCAGAGGTTGCAGTGAGCCGAGATGGCGCCACTGGACTCTAGCCTGGGCAACAAGAGTGAAATTCTGCCTCAGAAAAAAAAAAAAAAAAAAAAAAAAGATGCTTTTCCTTCACTACAGTGTTCTTCTCTGAAACTCTTTAATCTGAAAGTTTAGAAGTTCA... | ACGCATTTCTCTTGTTTATCTGTCTCTTGTTCTAGGGGCCTCAGCTGTGAACTTGGATGGGTGAGGAAAAGATATTTTTCCTGGCTGGGCAAGGTGGCTCACGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCATGAGGCAGAGGTTGCAGTGAGCCGAGATGGCGCCACTGGACTCTAGCCTGGGCAACAAGAGTGAAATTCTGCCTCAGAAAAAAAAAAAAAAAAAAAAAAAAGATGCTTTTCCTTCACTACAGTGTTCTTCTCTGAAACTCTTTAATCTGAAAGTTTAGAAGTTCA... |
Task1_train_34498 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GAGGAGGCAGGTGGCCCTCCTCGGCAGGAGGTGAGCCGCCAGGGAGGGATGGGGGTCACCCAAGCCCCTGCAAGCGCGACCCTGCCCAGAGCAAAGCACGCCCCGCGCCTGGTGAGGAACTTTTTCTTTCCAAAGGTGGCAGGAACAAGTCTGTACTGACTTTTCTCCCGCCTTCGGGATCCTCTCTCGTATGATTTGTGGTTTGTGGGACCACAACAACCAGGCTTCCTCGACCGCGCCTTTTTTCCAGTAGCTCCTGGTCTGCCAGGCTTGCGAGAGGGCGCGCTGGCTTGGCGGGGCTCCGGGCGAGAAATCACCAG... | GAGGAGGCAGGTGGCCCTCCTCGGCAGGAGGTGAGCCGCCAGGGAGGGATGGGGGTCACCCAAGCCCCTGCAAGCGCGACCCTGCCCAGAGCAAAGCACGCCCCGCGCCTGGTGAGGAACTTTTTCTTTCCAAAGGTGGCAGGAACAAGTCTGTACTGACTTTTCTCCCGCCTTCGGGATCCTCTCTCGTATGATTTGTGGTTTGTGGGACCACAACAACCAGGCTTCCTCGACCGCGCCTTTTTTCCAGTAGCTCCTGGTCTGCCAGGCTTGCGAGAGGGCGCGCTGGCTTGGCGGGGCTCCGGGCGAGAAATCACCAG... |
Task1_train_34499 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | CTCCTGGGTGGCCTGGGGAGAAGGGGGCGGGACAGCACAGCTTCTTCCCCTCGGGTGGGCATGACGGGTCGCCTTGGGTGTCCTGCCGAGCTCAGCTTTGAGGGTATGCGCGGCGCGGGTGTTTTTCCCAGGTCCACTCTGCAAAAGTTGTGGCCTGAGGAAAACTTCCAGGTCGCCAGCAGGAACGTCACAGGAGAGCCCCGGTCGCTCGTCAGGCGGGCGGCCCTGGAGCGTGCGCGCCACCCAACGCCGCGCTGGGCGGCCGCCCGGCCCCGCCCCAGGTCACAGCCCTGCCCTCGGCCCCACCGCGGCGGGCGGGG... | CTCCTGGGTGGCCTGGGGAGAAGGGGGCGGGACAGCACAGCTTCTTCCCCTCGGGTGGGCATGACGGGTCGCCTTGGGTGTCCTGCCGAGCTCAGCTTTGAGGGTATGCGCGGCGCGGGTGTTTTTCCCAGGTCCACTCTGCAAAAGTTGTGGCCTGAGGAAAACTTCCAGGTCGCCAGCAGGAACGTCACAGGAGAGCCCCGGTCGCTCGTCAGGCGGGCGGCCCTGGAGCGTGCGCGCCACCCAACGCCGCGCTGGGCGGCCGCCCGGCCCCGCCCCAGGTCACAGCCCTGCCCTCGGCCCCACCGCGGCGGGCGGGG... |
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